Drugs, Poisons and Controlled Substances Regulations 2006
i
Drugs, Poisons and Controlled Substances
Regulations 2006
S.R. No. 57/2006
TABLE OF PROVISIONS
Regulation Page
PART 1—PRELIMINARY 1
1. Objectives 1
2. Authorising provisions 2
3. Revocation 2
4. Definitions 2
PART 2—DRUGS OF DEPENDENCE, SCHEDULE 4 POISONS,
SCHEDULE 8 POISONS AND SCHEDULE 9 POISONS 5
Division 1—Possession 5
5. Possession of Schedule 4 poisons, Schedule 8 poisons and
Schedule 9 poisons 5
6. Approval of Schedule 4 poisons and Schedule 8 poisons 12
7. Permit required for Schedule 9 poisons 13
Division 2—Treatment 13
8. Patient identity and therapeutic need to be determined—
registered medical practitioners 13
9. Patient identity and therapeutic need to be determined—nurse
practitioners 14
10. Patient identity and therapeutic need to be determined—
dentists 14
11. Therapeutic need to be determined—authorised optometrists 15
12. Patient identity and therapeutic need to be determined for
drugs of dependence—pharmacists 15
13. Therapeutic need to be determined—veterinary practitioners 16
14. Notification of fraudulent obtaining of drugs or poisons 17
15. Pharmacist administration, sale or supply authorised from
within Victoria 18
16. Supply on copy of prescription permitted in certain
circumstances 20
17. Pharmacist administration, sale or supply authorised from outside
Victoria 20
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18. Form of notification under section 33(1) of the Act 21
19. Form of application and notification under sections 33(2)
and 33(3) of the Act 21
20. Form of permit under section 34 of the Act 21
21. Permit required in particular circumstances for specialised
supply 21
22. Permit required in particular circumstances for specialised
supply 22
23. Dentists not able to obtain permit for specialised supply 23
24. Disclosure of drug use within previous 8 weeks required 23
Division 3—Supply 24
25. Persons authorised to write prescriptions 24
26. Style and required particulars for prescriptions 25
27. Emergency directions to pharmacists regarding supply 28
28. Particular prescription details to be verified prior to supply 29
29. Containers of drugs to be labelled with certain details 29
30. Duration of prescriptions 33
31. Circumstances where prescriptions are not to be filled 34
32. Duty of pharmacist to notify different prescribers of similar
supply 34
33. Retention of original prescriptions or orders once supply
completed 35
Division 4—Storage 36
34. General security requirement—Schedule 4 poisons 36
35. Storage of Schedule 8 and Schedule 9 poisons 37
36. Storage requirements 39
37. Additional security provisions required in certain circumstances 40
Division 5—Records 42
38. Definition of transaction 42
39. Persons required to keep records 42
40. Details to be contained in records 43
41. Methods by which records are to be retained and retrieved 44
42. Accurate records to be kept 46
43. Discrepancies in records to be investigated 46
44. Lost or stolen records to be reported 46
Division 6—Administration 47
45. Use of drugs and poisons restricted to person or animal for
whom they were supplied 47
46. Administration of drugs and poisons to be authorised 47
47. Administration of drugs and poisons by a nurse 49
48. Self-administration of drugs and poisons restricted 52
49. Administration or supply of drugs and poisons prohibited if
to support drug dependency 53
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Division 7—Destruction of Schedule 8 Poisons and Schedule 9
Poisons 53
50. Wilful destruction prohibited 53
51. Exceptions 53
Division 8—Cultivation of Narcotic Plants 56
52. Authority to cultivate narcotic plants for non-therapeutic uses 56
Division 9—Warrants for Ovulatory Stimulants, Prostaglandins,
Retinoids and Thalidomide 56
53. Requirement for warrants 56
54. Warrant number to be included in any prescription 57
55. Prohibition on dentists 57
PART 3—PRESCRIBED POISONS FOR CATEGORIES OF
NURSE PRACTITIONER 58
56. Prescribed poisons related to certain categories of nurse
practitioner 58
PART 4—SCHEDULE 3 POISONS 60
57. Therapeutic need to be determined—registered medical
practitioners 60
58. Therapeutic need to be determined—nurse practitioners 60
59. Therapeutic need to be determined—veterinary practitioners 60
60. Therapeutic need to be determined—dentists 61
61. Therapeutic need to be determined—pharmacists 61
62. Restrictions on storage and display 61
63. Requirements to supply 62
64. Administration or supply prohibited if to support drug
dependency 62
PART 5—SCHEDULE 7 POISONS 63
65. Controls concerning listed regulated poisons 63
66. Storage requirements 63
67. Licences, permits or warrants required for special Schedule 7
substances 63
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PART 6—GENERAL REQUIREMENTS 64
68. Poisons to be sold by wholesale and retail in original unopened
packs 64
69. Transfer of poisons to inappropriate containers prohibited 64
70. Lost or stolen poisons to be notified 65
71. Access to certain poisons restricted to a needs basis 66
72. Form of seizure notice under section 43(1) of the Act 66
73. Form of complaint notice against a seizure under section 43(2)
of the Act 66
PART 7—LICENCES AND PERMITS ISSUED UNDER THE ACT 67
74. Licence to sell or supply Schedule 2 poisons by retail 67
75. Fees 67
PART 8—TRANSITIONALS 75
76. Continuity of approvals, authorisations and directions 75
__________________
SCHEDULES 77
SCHEDULE 1—Revoked Statutory Rules 77
SCHEDULE 2—Forms 79
Form DP1—Notification of Drug Dependent Person 79
Form DP2—Treatment with Schedule 8 Poisons or Schedule 9
Poisons by a Registered Medical Practitioner or
Schedule 8 Poisons by a Nurse Practitioner 80
Form DP3—Permit to Administer, Prescribe or Supply a Schedule 8
Poison or Schedule 9 Poison by a Registered medical
practitioner or a Schedule 8 Poison by a Nurse
Practitioner 83
Form DP4—Notice of Seizure 84
Form DP5—Notice of Complaint in Respect of a Seizure 85
SCHEDULE 3 86
═══════════════
ENDNOTES 90
INDEX 92
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1
STATUTORY RULES 2006
S.R. No. 57/2006
Drugs, Poisons and Controlled Substances Act 1981
Drugs, Poisons and Controlled Substances
Regulations 2006
The Governor in Council makes the following Regulations:
Dated: 25 May 2006
Responsible Minister:
BRONWYN PIKE
Minister for Health
RUTH LEACH
Clerk of the Executive Council
PART 1—PRELIMINARY
1. Objectives
The objectives of these Regulations are to—
(a) facilitate and enhance the orderly sale,
supply, prescribing, administration and use
of drugs, poisons and controlled substances
by health professionals, authorised persons,
licensed or permitted persons and the general
public; and
(b) prescribe fees relating to the provision of
licences and permits issued under the Drugs,
Poisons and Controlled Substances Act
1981; and
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(c) prescribe forms and other matters necessary
to be prescribed for the purposes of the
Drugs, Poisons and Controlled Substances
Act 1981.
2. Authorising provisions
These Regulations are made under sections 129,
131, 132, 132A and 132B of the Drugs, Poisons
and Controlled Substances Act 1981.
3. Revocation
The regulations set out in Schedule 1 are revoked.
4. Definitions
In these Regulations—
"aged care service" has the same meaning as it
has in the Aged Care Act 1997 of the
Commonwealth;
"animal" includes any bird, fish or insect;
"approved" means approved in writing by the
Secretary;
"approved provider" has the same meaning as it
has in the Aged Care Act 1997 of the
Commonwealth;
"Australian Orthoptic Board" means a
committee constituted of the directors of the
Australian Orthoptists Registration Body
Pty Ltd;
"authorised optometrist" means a registered
optometrist whose registration is endorsed
under section 11 of the Optometrists
Registration Act 1996;
"high level of residential care" has the same
meaning as it has in the Aged Care Act 1997
of the Commonwealth;
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"listed regulated poison" means a Schedule 7
poison that is included in Part 2 of Chapter 1
of the Poisons Code in the list of substances
that are not for general sale by retail;
"nurse" means—
(a) a person registered in division 1,
division 3 or division 4 of the register
of nurses established under the Nurses
Act 1993; or
(b) a person registered in division 2 of that
register whose registration is endorsed
under section 8C of that Act;
"orthoptist" means a person who is registered as
an orthoptist with the Australian Orthoptic
Board;
"ovulatory stimulant" means a substance listed
as an ovulatory stimulant in Part 2 of
Chapter 1 of the Poisons Code;
"palliative care service" means a service which
provides medical and nursing care to persons
who are terminally ill;
"pharmacy" has the same meaning as it has in
the Pharmacy Practice Act 2004;
"pharmacy business" has the same meaning as it
has in the Pharmacy Practice Act 2004;
"pharmacy department" has the same meaning
as it has in the Pharmacy Practice Act
2004;
"podiatrist" means a person registered as a
podiatrist under the Podiatrists Registration
Act 1997;
"prostaglandin" means a substance listed as a
prostaglandin in Part 2 of Chapter 1 of the
Poisons Code;
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"registered dental auxiliary" has the same
meaning as it has in the Dental Practice Act
1999;
"retinoid" means a substance listed as a retinoid
in Part 2 of Chapter 1 of the Poisons Code;
"special Schedule 7 substance" means a
substance listed as a special Schedule 7
substance in Part 2 of Chapter 1 of the
Poisons Code;
"storage facility" includes a cabinet, receptacle,
cupboard, refrigerator or room;
"the Act" means the Drugs, Poisons and
Controlled Substances Act 1981.
__________________
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PART 2—DRUGS OF DEPENDENCE, SCHEDULE 4
POISONS, SCHEDULE 8 POISONS AND SCHEDULE 9
POISONS
Division 1—Possession
5. Possession of Schedule 4 poisons, Schedule 8 poisons
and Schedule 9 poisons
(1) A person or class of persons shown in an item in
Column 1 of the following table is authorised to
have in his or her possession a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison to the
extent shown in Column 2.
TABLE
Column 1 Column 2
PART 1
1. A person who holds or
who is the agent of a
person who holds a
licence, permit or
warrant issued under the
Act or these Regulations.
Those Schedule 4
poisons, Schedule 8
poisons or Schedule 9
poisons named on the
licence, permit or
warrant to the extent
and for the purpose
specified in the
licence, permit or
warrant.
2. A person who is a
carrier, a carrier's
employee or a
messenger.
For the purposes of
delivery to the person
to whom the
consignment is
addressed, those
Schedule 4 poisons,
Schedule 8 poisons or
Schedule 9 poisons
consigned by—
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Column 1 Column 2
(a) a person holding
a licence or
permit under the
Act or these
Regulations; or
(b) in the case of a
Schedule 9
poison, a
registered
medical
practitioner,
pharmacist,
veterinary
practitioner or
dentist; or
(c) in the case of a
Schedule 8
poison, a
registered
medical
practitioner,
pharmacist,
veterinary
practitioner,
dentist or nurse
practitioner; or
(d) in the case of a
Schedule 4
poison, a
registered
medical
practitioner,
pharmacist,
veterinary
practitioner,
dentist or nurse
practitioner; or
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Column 1 Column 2
(e) in the case of a
Schedule 4
poison specified
in his or her
endorsement of
registration, an
authorised
optometrist.
3. A person for whom a
Schedule 9 poison has
been supplied by a
registered medical
practitioner, pharmacist
or dentist in accordance
with the Act and these
Regulations.
That Schedule 9
poison to the extent
and for the purpose
for which it is
supplied.
4. A person for whom a
Schedule 8 poison has
been supplied by a
registered medical
practitioner, pharmacist,
dentist or nurse
practitioner in
accordance with the Act
and these Regulations.
That Schedule 8
poison to the extent
and for the purpose
for which it is
supplied.
5. A person for whom a
Schedule 4 poison has
been supplied by a
registered medical
practitioner, pharmacist,
dentist or nurse
practitioner in
accordance with the Act
and these Regulations.
That Schedule 4
poison to the extent
and for the purpose
for which it was
supplied.
6. A person for whom a
Schedule 4 poison has
been supplied in
accordance with the Act
and these Regulations by
an authorised optometrist
whose endorsement of
registration specifies that
Schedule 4 poison.
That Schedule 4
poison to the extent
and for the purpose
for which it is
supplied.
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Column 1 Column 2
7. The agent or a person
who has the care of, or
who is assisting in the
care of, a person referred
to in item 3, 4, 5 or 6.
That Schedule 4
poison, Schedule 8
poison, or Schedule 9
poison to the extent
and for the purpose
for which it is
supplied.
8. An owner of, or a person
having custody or care
of, an animal for which a
Schedule 4 poison or
Schedule 8 poison has
been supplied by a
veterinary practitioner or
pharmacist in accordance
with the Act and these
Regulations.
That Schedule 4
poison or Schedule 8
poison to the extent
and for the purpose
for which it is
supplied.
9. An owner or person
having custody or care of
a flock or herd of
animals for which a
Schedule 4 poison has
been supplied by
wholesale in a stockfeed
on the order of a
veterinary practitioner
for the treatment of that
flock or herd of animals
in accordance with the
Act or these Regulations.
That Schedule 4
poison to the extent
and for the purpose
for which it is
supplied.
PART 2
10. An operational staff
member within the
meaning of the
Ambulance Services
Act 1986.
Those Schedule 4
poisons or Schedule 8
poisons listed in the
health services permit
held by that
ambulance service
within the meaning of
the Ambulance
Services Act 1986.
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Column 1 Column 2
11. A member of St John
Ambulance Australia
(Vic.) recognised by that
organisation as qualified
to Advanced First Aid
level.
Those Schedule 4
poisons listed in the
health services permit
held by St John
Ambulance Australia
(Vic.).
12. A master or chief officer
of a ship in port in
Victoria.
Those Schedule 4
poisons or Schedule 8
poisons that are
required by State,
Commonwealth or
international law to
complete the
equipment of that
ship.
13. A yacht owner or crew
member who is a
member of Yachting
Australia and whose
yacht is entered in a race
conducted under the
rules of Yachting
Australia.
Those Schedule 4
poisons or Schedule 8
poisons contained in
the Medical Kit for
the Yachting
Australia Race
Category in which the
yacht is entered.
14. A registered optometrist
carrying on the lawful
practice of his or her
profession.
Those Schedule 4
poisons approved by
the Secretary that are
required in the
practice of his or her
profession for use in
the eyes of patients.
15. A podiatrist carrying on
the lawful practice of his
or her profession.
Those Schedule 4
poisons approved by
the Secretary that are
required in the
practice of his or her
profession for the
treatment of
conditions of the
human foot.
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Column 1 Column 2
16. A person who holds a
permit to use etorphine
in accordance with the
Act and these
Regulations or a person
assisting that permit
holder.
Those morphine
antagonists that are
necessary for
administration as an
antidote to etorphine.
17. An Australian Ski Patrol
Association Inc.
qualified ski patroller.
Those Schedule 4
poisons approved by
the Secretary that are
required in the
performance of a ski
patroller's duties for
the treatment of
emergencies.
18. A Director of State
Emergency Services.
Those Schedule 4
poisons or Schedule 8
poisons that are
required in the
performance of his or
her duties in an
emergency coming
within his or her
jurisdiction.
19. A municipal council, an
environmental health
officer or a nurse
employed or appointed
by a municipal council.
Those Schedule 4
poisons that are
necessary for
immunisation
programs coordinated
by a municipal
council in accordance
with its functions
under the Health Act
1958.
20. A registered dental
auxiliary.
Those Schedule 4
poisons approved by
the Secretary that are
required for the
provision of dental
care by the registered
dental auxiliary.
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Column 1 Column 2
21. An orthoptist practising
under the direction of a
registered medical
practitioner or an
authorised optometrist.
Those Schedule 4
poisons that are local
anaesthetics and
cycloplegics in topical
ophthalmic
preparations for the
use in the eyes of
patients.
(2) A nurse is authorised to possess those Schedule 4
poisons, Schedule 8 poisons or Schedule 9
poisons that are necessary for administration to a
patient under the care of that nurse in accordance
with—
(a) the instructions of and upon the authorisation
for that patient by—
(i) in the case of a Schedule 4 poison,
Schedule 8 poison or Schedule 9
poison, a registered medical
practitioner or dentist; or
(ii) in the case of a Schedule 4 poison or
Schedule 8 poison, a nurse practitioner;
or
(iii) in the case of a Schedule 4 poison
specified in his or her endorsement of
registration, an authorised optometrist;
or
(b) the conditions of a permit to purchase or
obtain and use a poison or controlled
substance for the provision of health
services; or
(c) the approval of the Secretary under sub-
regulation (3).
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(3) Subject to sub-regulation (4), the Secretary may
approve the possession of a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison by a
nurse or class of nurses without the direct
supervision of—
(a) in the case of a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison, a
registered medical practitioner or dentist; or
(b) in the case of a Schedule 4 poison or
Schedule 8 poison, a nurse practitioner; or
(c) in the case of a Schedule 4 poison specified
in his or her endorsement of registration, an
authorised optometrist.
(4) The Secretary must not grant an approval referred
to in sub-regulation (3) unless the Secretary
considers that the approval—
(a) is necessary for the provision of health
services; and
(b) is within the competence of a nurse without
the direct supervision of a registered medical
practitioner, dentist, nurse practitioner or
authorised optometrist (as the case requires).
6. Approval of Schedule 4 poisons and Schedule 8
poisons
The Secretary may approve Schedule 4 poisons or
Schedule 8 poisons or classes of Schedule 4
poisons or Schedule 8 poisons for possession and
use by a person or class of persons specified in
Column 1 of Part 2 of the table in Regulation 5.
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7. Permit required for Schedule 9 poisons
A registered medical practitioner, pharmacist,
veterinary practitioner or dentist must not
manufacture, sell, supply, purchase or otherwise
obtain, possess, administer, use or prescribe a
Schedule 9 poison unless he or she holds a permit
issued under the Act or these Regulations to do so.
Penalty: 100 penalty units.
Division 2—Treatment
8. Patient identity and therapeutic need to be
determined—registered medical practitioners
(1) A registered medical practitioner must not
administer, prescribe, sell or supply a drug of
dependence or Schedule 8 poison unless—
(a) that drug or poison is for the medical
treatment of a person under his or her care;
and
(b) he or she has taken all reasonable steps to
ascertain the identity of that person; and
(c) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that drug
or poison.
Penalty: 100 penalty units.
(2) A registered medical practitioner must not
administer, prescribe, sell or supply a Schedule 4
poison unless—
(a) that poison is for the medical treatment of a
person under his or her care; and
(b) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that
poison.
Penalty: 100 penalty units.
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9. Patient identity and therapeutic need to be
determined—nurse practitioners
(1) A nurse practitioner must not administer,
prescribe, sell or supply a Schedule 8 poison
unless—
(a) that poison is for the treatment of a person
under his or her care; and
(b) he or she has taken all reasonable steps to
ascertain the identity of that person; and
(c) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that
poison.
Penalty: 100 penalty units.
(2) A nurse practitioner must not administer,
prescribe, sell or supply a Schedule 4 poison
unless—
(a) that poison is for the treatment of a person
under his or her care; and
(b) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that
poison.
Penalty: 100 penalty units.
10. Patient identity and therapeutic need to be
determined—dentists
(1) A dentist must not administer, prescribe, sell or
supply a drug of dependence or Schedule 8 poison
unless—
(a) that drug or poison is for the dental treatment
of a person under his or her care; and
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(b) he or she has taken all reasonable steps to
ascertain the identity of that person; and
(c) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that drug
or poison.
Penalty: 100 penalty units.
(2) A dentist must not administer, prescribe, sell or
supply a Schedule 4 poison unless—
(a) that poison is for the dental treatment of a
person under his or her care; and
(b) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that
poison.
Penalty: 100 penalty units.
11. Therapeutic need to be determined—authorised
optometrists
An authorised optometrist must not administer,
prescribe, sell or supply a Schedule 4 poison
unless—
(a) that poison is for the ocular treatment of a
person under his or her care; and
(b) the optometrist has taken all reasonable steps
to ensure a therapeutic need exists for that
poison.
Penalty: 100 penalty units.
12. Patient identity and therapeutic need to be
determined for drugs of dependence—pharmacists
(1) A pharmacist who supplies a drug of dependence
to or for a person other than by wholesale or on
the prescription of a registered medical
practitioner, dentist or nurse practitioner must—
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(a) take all reasonable steps to ascertain the
identity of the person to or for whom it is
proposed to supply the drug of dependence;
and
(b) do so only for the therapeutic use of the
person after having taken all reasonable steps
to ensure a therapeutic need for the drug of
dependence exists.
Penalty: 100 penalty units.
(2) A pharmacist who supplies a drug of dependence
to a person for an animal other than by wholesale
or on the prescription of a veterinary practitioner
must do so only for the therapeutic use of the
animal after having taken all reasonable steps to
ensure a therapeutic need for the drug of
dependence exists.
Penalty: 100 penalty units.
13. Therapeutic need to be determined—veterinary
practitioners
A veterinary practitioner must not administer,
prescribe, sell or supply a drug of dependence,
Schedule 8 poison or Schedule 4 poison unless—
(a) that drug or poison is for the treatment of an
animal under his or her care; and
(b) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that drug
or poison.
Penalty: 100 penalty units.
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14. Notification of fraudulent obtaining of drugs or
poisons
(1) A registered medical practitioner, pharmacist,
veterinary practitioner or dentist who suspects or
has reason to believe that a person has obtained
from him or her by means of a false pretence—
(a) a drug of dependence, Schedule 9 poison,
Schedule 8 poison or Schedule 4 poison; or
(b) an order or prescription for a drug of
dependence, Schedule 9 poison, Schedule 8
poison or Schedule 4 poison—
must immediately inform the Secretary and a
member of the Victoria Police of that suspicion or
belief.
Penalty: 50 penalty units.
(2) A nurse practitioner who suspects or has reason to
believe that a person has obtained from him or her
by means of a false pretence—
(a) a Schedule 8 poison or Schedule 4 poison; or
(b) an order or prescription for a Schedule 8
poison or Schedule 4 poison—
must immediately inform the Secretary and a
member of the Victoria Police of that suspicion or
belief.
Penalty: 50 penalty units.
(3) An authorised optometrist who suspects or has
reason to believe that a person has obtained from
him or her by means of a false pretence, a
Schedule 4 poison or an order or prescription for a
Schedule 4 poison, must immediately inform the
Secretary and a member of the Victoria Police of
that suspicion or belief.
Penalty: 50 penalty units.
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15. Pharmacist administration, sale or supply
authorised from within Victoria
(1) A pharmacist must not administer, sell or supply a
Schedule 4 poison or Schedule 8 poison except—
(a) in accordance with section 13(3) of the Act;
or
(b) subject to regulation 16, on the original
prescription of—
(i) in the case of a Schedule 8 poison, a
registered medical practitioner,
veterinary practitioner, dentist or nurse
practitioner;
(ii) in the case of a Schedule 4 poison, a
registered medical practitioner,
veterinary practitioner, dentist or nurse
practitioner;
(iii) in the case of a Schedule 4 poison
specified in his or her endorsement of
registration, an authorised optometrist;
or
(c) in accordance with regulation 27; or
(d) in the case of a Schedule 8 poison, on the
order of a registered medical practitioner,
veterinary practitioner, dentist or nurse
practitioner; or
(e) in the case of a Schedule 4 poison, on the
order of—
(i) a registered medical practitioner,
veterinary practitioner, dentist or nurse
practitioner; or
(ii) an authorised optometrist, in
accordance with his or her endorsement
of registration; or
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(f) on the order of a person holding a permit for
that Schedule 4 poison or Schedule 8 poison;
or
(g) to a person referred to in Column 1 of Part 2
of the table in regulation 5 to the extent
referred to in Column 2 of that Part of that
Table.
Penalty: 100 penalty units.
(2) Despite sub-regulation (1), in an emergency, a
pharmacist may, if he or she considers it necessary
to ensure continuity of treatment, supply once
only a Schedule 4 poison without the prescription
of a registered medical practitioner or nurse
practitioner if—
(a) the pharmacist is satisfied that—
(i) there is an immediate need for the
Schedule 4 poison and it is
impracticable for the patient to obtain a
prescription in time to meet that need;
and
(ii) treatment with that Schedule 4 poison
has been previously prescribed for the
patient by a registered medical
practitioner or nurse practitioner; and
(iii) the patient, or the agent of the patient,
or a person who has the care of, or is
assisting in the care of, the patient, is
aware of the appropriate dose of that
Schedule 4 poison for that patient; and
(b) the quantity supplied does not exceed—
(i) 3 days' supply; or
(ii) if it is not practical to supply a quantity
required for 3 days, the smallest
commercially available pack.
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16. Supply on copy of prescription permitted in certain
circumstances
(1) Subject to sub-regulation (2), a pharmacist may
supply a Schedule 4 poison or a Schedule 8 poison
on the copy of an original prescription if the
original prescription is required to be submitted to
a public authority by any Act of a State or
Territory or the Commonwealth.
(2) A pharmacist must not supply a Schedule 4 poison
or a Schedule 8 poison on the copy of an original
prescription unless the copy of the original
prescription is certified by or accompanied by a
certification from—
(a) the pharmacist who received the original
prescription but did not supply all of the
items on that prescription; or
(b) a pharmacist who has previously supplied
the Schedule 4 poison or Schedule 8 poison
on that original prescription.
Penalty: 100 penalty units.
17. Pharmacist administration, sale or supply
authorised from outside Victoria
Despite regulation 15, a pharmacist may supply a
Schedule 4 poison on the prescription of a person
who is registered in another State or Territory as a
person who is—
(a) permitted to practice medicine, nursing,
veterinary science, dentistry or optometry;
and
(b) permitted by a law of that State or Territory
to prescribe Schedule 4 poisons.
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18. Form of notification under section 33(1) of the Act
For the purposes of section 33(1) of the Act, the
prescribed form is the form of DP1 in Schedule 2.
19. Form of application and notification under
sections 33(2) and 33(3) of the Act
For the purposes of sections 33(2) and 33(3) of the
Act, the prescribed form is the form of DP2 in
Schedule 2.
20. Form of permit under section 34 of the Act
For the purposes of section 34 of the Act, the
prescribed form is the form of DP3 in Schedule 2.
21. Permit required in particular circumstances for
specialised supply
(1) For the purposes of preventing the improper use
of methadone, a registered medical practitioner or
nurse practitioner must not administer, supply or
prescribe methadone in circumstances where the
registered medical practitioner or nurse
practitioner is not required to hold a permit under
section 34(1) of the Act unless he or she has a
permit from the Secretary authorising that
registered medical practitioner or nurse
practitioner to administer, supply or prescribe
methadone.
Penalty: 100 penalty units.
(2) Despite sub-regulation (1), a registered medical
practitioner or nurse practitioner is not required to
have a permit under this regulation if—
(a) the person he or she is treating is an inpatient
of a hospital; or
(b) he or she is treating a patient at an oncology
clinic or a pain clinic at a hospital; or
(c) he or she is treating a patient who is under
the care of a palliative care service.
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(3) The form of an application for a permit under sub-
regulation (1) authorising the administration,
supply or prescription of methadone, is the form
of DP2 in Schedule 2.
(4) A permit referred to in sub-regulation (1)
authorising the administration, supply or
prescription of methadone is subject to the terms
and conditions specified in the permit by the
Secretary.
22. Permit required in particular circumstances for
specialised supply
(1) For the purposes of preventing the improper use
of amphetamine, dexamphetamine,
methylamphetamine or methylphenidate, a
registered medical practitioner or nurse
practitioner must not administer, supply or
prescribe any one or more of those substances in
circumstances where the registered medical
practitioner or nurse practitioner is not required to
hold a permit under section 34(1) of the Act
unless he or she has a permit from the Secretary
authorising that registered medical practitioner or
nurse practitioner to administer, supply or
prescribe one or more of those substances.
Penalty: 100 penalty units.
(2) Despite sub-regulation (1), a registered medical
practitioner is not required to have a permit under
this regulation if he or she is—
(a) a paediatrician who is treating a person for
attention deficit disorder; or
(b) a psychiatrist who is treating a person for
attention deficit disorder.
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(3) The form of an application for a permit under sub-
regulation (1) authorising the administration,
supply or prescription of amphetamine,
dexamphetamine, methylamphetamine or
methylphenidate is the form of DP2 in Schedule 2.
(4) A permit referred to in sub-regulation (1)
authorising the administration, supply or
prescription of amphetamine, dexamphetamine,
methylamphetamine or methylphenidate is subject
to the terms and conditions specified in the permit
by the Secretary.
23. Dentists not able to obtain permit for specialised
supply
A dentist must not possess, administer, supply or
prescribe methadone.
Penalty: 100 penalty units.
24. Disclosure of drug use within previous 8 weeks
required
(1) A person who in the previous 8 weeks has been
treated with a drug of dependence must not,
without disclosing that fact at the time, procure or
attempt to procure from a registered medical
practitioner, veterinary practitioner, dentist or
nurse practitioner—
(a) the same or a similar drug of dependence; or
(b) a drug of dependence for the same or a
similar purpose.
Penalty: 100 penalty units.
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(2) A person who in the previous 8 weeks has been
treated with a drug of dependence must not,
without disclosing that fact at the time, procure or
attempt to procure from a pharmacist, other than
on a prescription or order of a person authorised in
relation to that drug of dependence under
section 13(1) of the Act—
(a) the same or a similar drug of dependence; or
(b) a drug of dependence for the same or a
similar purpose.
Penalty: 100 penalty units.
Division 3—Supply
25. Persons authorised to write prescriptions
(1) A person other than a registered medical
practitioner, veterinary practitioner or dentist must
not write a prescription for a Schedule 9 poison.
Penalty: 100 penalty units.
(2) A person other than a registered medical
practitioner, veterinary practitioner, dentist or
nurse practitioner must not write a prescription for
a Schedule 8 poison.
Penalty: 100 penalty units.
(3) A person other than a registered medical
practitioner, veterinary practitioner, dentist, nurse
practitioner or authorised optometrist must not
write a prescription for a Schedule 4 poison.
Penalty: 100 penalty units.
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(4) A registered medical practitioner or dentist must
not write a prescription for a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison other than
for the treatment of a person named on the
prescription.
Penalty: 100 penalty units.
(5) A nurse practitioner must not write a prescription
for a Schedule 4 poison or Schedule 8 poison
other than for the treatment of a person named on
the prescription.
Penalty: 100 penalty units.
(6) An authorised optometrist must not write a
prescription for a Schedule 4 poison other than for
the treatment of a person named on the
prescription.
Penalty: 100 penalty units.
(7) A veterinary practitioner must not write a
prescription for a Schedule 4 poison, Schedule 8
poison or Schedule 9 poison other than for the
treatment of an animal named or described on the
prescription.
Penalty: 100 penalty units.
26. Style and required particulars for prescriptions
(1) A person authorised to write a prescription under
regulation 25 must write a prescription for a
Schedule 4 poison, Schedule 8 poison or
Schedule 9 poison (as the case requires)—
(a) in his or her own handwriting; or
(b) in a manner of writing approved by the
Secretary.
Penalty: 50 penalty units.
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(2) In approving another manner of writing a
prescription under sub-regulation (1)(b), the
Secretary—
(a) must have regard to security; and
(b) must have regard to legibility; and
(c) may have regard to any other factors the
Secretary considers relevant in the
circumstances.
(3) A person authorised to write a prescription under
regulation 25 must ensure that any prescription
written by the person for a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison (as the
case requires) is legible and durable and
includes—
(a) the name, address and telephone number of
the prescriber; and
(b) the name and address of the patient for
whom the prescription is intended, or if a
prescription is written by a veterinary
practitioner, the name or species of animal
and the name and address of the owner or the
person having the custody of the animal; and
(c) the date on which the prescription was
written; and
(d) the signature of the prescriber; and
(e) full particulars of the poison or controlled
substance to be supplied including a
statement of the quantity to be supplied; and
(f) in the case of a Schedule 8 poison or
Schedule 9 poison, the statement of the
quantity to be supplied written in words and
figures; and
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(g) directions for the precise dose or use and
frequency of administration except in cases
where—
(i) because of the complexity of the dosage
regimen or use it is impracticable to do
so and the prescriber has separately
supplied the patient with written
instruction; or
(ii) the administration of the poison or
controlled substance is to be carried out
by a registered medical practitioner,
veterinary practitioner, pharmacist,
dentist, authorised optometrist or nurse
as the case requires; and
(h) the maximum number of times the
prescription may be supplied if more than
once; and
(i) in the case of a Schedule 8 poison or
Schedule 9 poison, the maximum number of
times the prescription may be supplied
written in words and figures.
Penalty: 50 penalty units.
(4) A prescription for a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison must not
be written in a secret code or cipher.
Penalty: 50 penalty units.
(5) A prescriber must not knowingly include on a
prescription for a Schedule 4 poison, Schedule 8
poison or Schedule 9 poison any particular which
is false or misleading.
Penalty: 100 penalty units.
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(6) A dentist must not direct that a prescription for a
Schedule 4 poison, Schedule 8 poison or
Schedule 9 poison be supplied more than once.
Penalty: 50 penalty units.
27. Emergency directions to pharmacists regarding
supply
(1) Despite anything in this Division to the contrary, a
registered medical practitioner, veterinary
practitioner or dentist may issue oral instructions
to a pharmacist to supply a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison if in the
opinion of the registered medical practitioner,
veterinary practitioner or dentist, an emergency
exists.
(2) Despite anything in this Division to the contrary, a
nurse practitioner may issue oral instructions to a
pharmacist to supply a Schedule 4 poison or
Schedule 8 poison if, in the opinion of the nurse
practitioner, an emergency exists.
(3) Despite anything in this Division to the contrary,
an authorised optometrist may issue oral
instructions to a pharmacist to supply a
Schedule 4 poison if, in the opinion of the
authorised optometrist, an emergency exists.
(4) A registered medical practitioner, veterinary
practitioner, dentist, nurse practitioner or
authorised optometrist who issues oral instructions
pursuant to sub-regulation (1), (2) or (3), as the
case requires, must as soon as practicable write a
prescription—
(a) indicating that it is in confirmation of the
oral instructions; and
(b) deliver or forward that prescription to the
pharmacist.
Penalty: 50 penalty units.
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28. Particular prescription details to be verified prior to
supply
(1) A pharmacist must not supply a Schedule 8 poison
or Schedule 9 poison on a prescription unless he
or she—
(a) if the prescription is handwritten, is familiar
with the purported prescriber's handwriting
and the writing is comparable with the usual
writing of the purported prescriber; or
(b) has taken reasonable steps to verify that the
prescription was written by the purported
prescriber.
Penalty: 100 penalty units.
(2) Despite sub-regulation (1), a pharmacist may
supply a quantity of a Schedule 8 poison sufficient
for no more than 2 days' treatment.
(3) A pharmacist who supplies a Schedule 8 poison in
accordance with sub-regulation (2) must retain the
prescription despite the full quantity ordered not
having been supplied.
Penalty: 100 penalty units.
29. Containers of drugs to be labelled with certain
details
(1) A registered medical practitioner, pharmacist,
veterinary practitioner or dentist who supplies a
Schedule 4 poison, Schedule 8 poison or
Schedule 9 poison for the treatment of a specific
person, or the veterinary treatment of a specific
animal, must ensure that the container in which it
is packed is labelled with the following
information—
(a) the name of the patient or name or species of
animal and the name of the owner or person
having custody of the animal; and
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(b) the date of recording as required by
Division 5; and
(c) the name, address and telephone number of
the place of supply; and
(d) the name of the poison or controlled
substance or a trade name which
unambiguously identifies the poison or
controlled substance and its strength, form
and quantity; and
(e) subject to sub-regulation (2), the directions
for use.
Penalty: 50 penalty units.
(2) A registered medical practitioner, pharmacist,
veterinary practitioner or dentist who supplies a
Schedule 4 poison, Schedule 8 poison or
Schedule 9 poison in accordance with sub-
regulation (1) is not required to include directions
for use of the poison on a label on the container
if—
(a) in the case of a pharmacist—
(i) directions for use have not been
included by the prescriber on the
prescription for that poison; or
(ii) the dosage regimen or use is so
complex that the prescriber has
supplied the patient with separate
written instruction; or
(b) the dosage regimen or use is so complex that
the registered medical practitioner,
veterinary practitioner or dentist has supplied
the patient with separate written instruction;
or
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(c) the administration of the poison is to be
carried out by a registered medical
practitioner, pharmacist, veterinary
practitioner, dentist, authorised optometrist
or nurse.
(3) A nurse practitioner who supplies a Schedule 4
poison or Schedule 8 poison for the treatment of a
specific person must ensure that the container in
which it is packed is labelled with the following
information—
(a) the name of the patient; and
(b) the date of recording as required by
Division 5; and
(c) the name, address and telephone number of
the place of supply; and
(d) the name of the poison or controlled
substance or a trade name which
unambiguously identifies the poison or
controlled substance and its strength, form
and quantity; and
(e) subject to sub-regulation (4), the directions
for use.
Penalty: 50 penalty units.
(4) A nurse practitioner who supplies a Schedule 4
poison or Schedule 8 poison in accordance with
sub-regulation (3) is not required to include
directions for use of the poison on a label on the
container if—
(a) the dosage regimen or use is so complex that
the nurse practitioner has supplied the patient
with separate written instruction; or
(b) the administration of the poison is to be
carried out by a registered medical
practitioner, pharmacist, dentist, authorised
optometrist or nurse.
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(5) An authorised optometrist who supplies a
Schedule 4 poison for the treatment of a specific
person must ensure that the container in which it
is packed is labelled with the following
information—
(a) the name of the patient; and
(b) the date of recording as required by
Division 5; and
(c) the name, address and telephone number of
the place of supply; and
(d) the name of the poison or controlled
substance or a trade name which
unambiguously identifies the poison or
controlled substance and its strength, form
and quantity; and
(e) subject to sub-regulation (6), the directions
for use.
Penalty: 50 penalty units.
(6) An authorised optometrist who supplies a
Schedule 4 poison in accordance with sub-
regulation (5) is not required to include directions
for use of the poison on a label on the container
if—
(a) the dosage regimen or use is so complex that
the authorised optometrist has supplied the
patient with separate written instruction; or
(b) the administration of the poison is to be
carried out by a registered medical
practitioner, pharmacist, dentist, authorised
optometrist or nurse.
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(7) A veterinary practitioner is not required to comply
with sub-regulation (1) if a Schedule 4 poison is
supplied in bulk for treatment of flocks or herds of
animals provided that—
(a) each container of the poison retains the
manufacturer's original label; and
(b) the veterinary practitioner provides written
instructions containing the information
specified in sub-regulation (1) to the owner
of, or the person having custody of, the
animals.
30. Duration of prescriptions
(1) A pharmacist who supplies a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison on a
prescription must ensure that the prescription is
marked in a way that indicates durably—
(a) that the poison or controlled substance has
been supplied; and
(b) the date of recording as required by
Division 5; and
(c) the premises from which the poison or
controlled substance was supplied.
Penalty: 50 penalty units.
(2) A pharmacist must not supply a Schedule 4
poison, Schedule 8 poison or Schedule 9 poison
on a prescription if it is more than—
(a) 12 months after the date written on the
prescription in the case of a prescription for a
Schedule 4 poison; or
(b) 6 months after the date written on the
prescription in the case of a prescription for a
Schedule 8 poison or Schedule 9 poison.
Penalty: 50 penalty units.
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31. Circumstances where prescriptions are not to be
filled
(1) A pharmacist must not supply a Schedule 4
poison, Schedule 8 poison or Schedule 9 poison
on a prescription—
(a) in excess of the quantities authorised; or
(b) which he or she has reason to believe has
been forged or is fraudulent in any way; or
(c) which he or she has reason to believe has
been altered in any way other than by or on
the instruction of the prescriber; or
(d) which is illegible or defaced; or
(e) when the quantity authorised has already
been supplied.
Penalty: 100 penalty units.
(2) A pharmacist to whom a prescription referred to
in sub-regulation (1)(b) or (c) is presented must
without delay notify a member of the Victoria
Police and the Secretary of the circumstances
concerning the presentation of the prescription.
Penalty: 50 penalty units.
32. Duty of pharmacist to notify different prescribers of
similar supply
A pharmacist who is presented with a prescription
for a drug of dependence or a Schedule 8 poison
or Schedule 9 poison for a person whom the
pharmacist has reason to believe was supplied in
the previous 8 weeks with the same or a similar
drug of dependence, Schedule 8 poison or
Schedule 9 poison on a prescription written by a
different prescriber must take all reasonable steps
prior to supply or, if unable to do so, as soon as
practicable after the supply has occurred, to
inform the prescriber that the previous supply has
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occurred unless the pharmacist has reason to
believe the prescriber is already aware of the
previous supply or prescription.
Penalty: 50 penalty units.
33. Retention of original prescriptions or orders once
supply completed
(1) A pharmacist who supplies a Schedule 8 poison or
Schedule 9 poison on a prescription or order of a
registered medical practitioner, veterinary
practitioner or dentist or a Schedule 8 poison on
the prescription or order of a nurse practitioner
must on the last occasion the supply is made—
(a) retain that prescription or order in a manner
that maintains the integrity of the
prescription or order; or
(b) in the case of a prescription or order on
which other poisons or controlled substances
may still be legally supplied, ensure that the
prescription or order is durably marked in
such a way that it can be seen clearly that
further supplies of that Schedule 8 poison or
Schedule 9 poison are not allowed.
Penalty: 50 penalty units.
(2) A pharmacist who retains a prescription or order
pursuant to sub-regulation (1)(a) must retain that
prescription or order on a file kept solely for the
purpose of retaining such prescriptions or orders
for a period of 3 years from the date the
Schedule 8 poison or Schedule 9 poison (as the
case requires) was last supplied.
(3) A pharmacist must produce a prescription or order
referred to in sub-regulation (2) on demand to an
authorised officer.
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(4) It is sufficient compliance with sub-regulation (1)
if a pharmacist retains a legible copy of the
prescription or order if he or she is required to
submit the original to a public authority by any
Act of a State, a Territory or the Commonwealth.
Division 4—Storage
34. General security requirement—Schedule 4 poisons
(1) A person to whom this regulation applies must
store any Schedule 4 poisons in the person's
possession in a lockable storage facility.
Penalty: 100 penalty units.
(2) A person to whom this regulation applies must
take all reasonable steps to ensure that the storage
facility referred to in sub-regulation (1) remains
locked and secured to prevent access by an
unauthorised person at all times, except—
(a) when it is necessary to open it to carry out an
essential operation in connection with the
poisons stored in it; or
(b) in the case of poisons stored in accordance
with sub-regulation (3)(a) or (b), when a
registered medical practitioner, pharmacist,
veterinary practitioner, dentist, nurse
practitioner, authorised optometrist or nurse
authorised under regulation 5(2)(a) is
present.
Penalty: 100 penalty units.
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(3) Despite sub-regulations (1) and (2), a registered
medical practitioner, pharmacist, veterinary
practitioner, dentist, nurse practitioner or
authorised optometrist may store Schedule 4
poisons at the premises in which he or she carries
out the lawful practice of his or her profession
in—
(a) the dispensing area or pharmacy department
of the premises; or
(b) the treatment room of the premises; or
(c) in an area separated from the remainder of
the premises and to which only a registered
medical practitioner, pharmacist, veterinary
practitioner, dentist, nurse practitioner or
authorised optometrist has access.
(4) This regulation applies to—
(a) a registered medical practitioner, pharmacist,
veterinary practitioner, dentist, nurse
practitioner and authorised optometrist; and
(b) a person holding a licence, permit or warrant
to manufacture, sell, supply, purchase or
otherwise obtain, possess, administer or use
a Schedule 4 poison; and
(c) a nurse approved under regulation 5(3) to be
in possession of a Schedule 4 poison.
35. Storage of Schedule 8 and Schedule 9 poisons
(1) A person to whom this regulation applies must
store any Schedule 8 poisons or Schedule 9
poisons in that person's possession in a lockable
storage facility that provides not less security than
a storage facility that is—
(a) constructed of mild steel plate of
10 millimetres thickness; and
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(b) constructed with continuous welding of all
edges; and
(c) fitted with a door constructed of mild steel
plate of 10 millimetres thickness, swung on
hinges welded to the door and body of the
cabinet, the door being flush fitting with a
clearance around the door of not more than
1⋅5 millimetres; and
(d) fitted with a fixed locking bar, welded to the
inside face of the door near the hinge edge,
which engages in a rebate when the door is
closed; and
(e) fitted with a 6 lever lock securely affixed to
the rear face of the door; and
(f) securely attached to a wall or floor in such a
manner that it will resist attack by hand tools
for 30 minutes or power tools for 5 minutes.
Penalty: 100 penalty units.
(2) A person to whom this regulation applies must
take all reasonable steps to ensure that the storage
facility remains locked and secured to prevent
access by an unauthorised person at all times,
except when it is necessary to open it to carry out
an essential operation in connection with the
poisons stored in it.
Penalty: 100 penalty units.
(3) A person to whom this regulation applies must
take all reasonable steps to ensure that the storage
facility referred to in sub-regulation (1) is used
only for the storage of Schedule 8 poisons,
Schedule 9 poisons and drugs of dependence.
Penalty: 100 penalty units.
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(4) A person to whom this regulation applies must
keep any Schedule 8 poisons or Schedule 9
poisons in the person's possession which are being
transported for use in another place in a locked
storage facility which is secured to prevent
unauthorised access to those poisons.
Penalty: 100 penalty units.
(5) Despite sub-regulations (1) and (3) a registered
medical practitioner or nurse practitioner may
keep up to 6 divided doses of a Schedule 8 poison
in a lockable storage facility for use in an
emergency.
(6) This regulation applies to—
(a) a registered medical practitioner, pharmacist,
veterinary practitioner, dentist and nurse
practitioner; and
(b) a person holding a licence, permit or warrant
to manufacture, sell, supply, purchase or
otherwise obtain, possess, administer or use
a Schedule 8 poison or a Schedule 9 poison;
and
(c) a nurse approved under regulation 5(3) to be
in possession of a Schedule 8 poison or a
Schedule 9 poison.
36. Storage requirements
(1) A person to whom this regulation applies must—
(a) store any Schedule 4 poison in the person's
possession in a lockable storage facility; and
(b) store any Schedule 8 poison or Schedule 9
poison in the person's possession in a
lockable room or in a lockable storage
facility which is firmly fixed to a floor or
wall; and
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(c) take all reasonable steps to ensure that the
storage facilities for Schedule 4 poisons,
Schedule 8 poisons and Schedule 9 poisons
remain locked and secured to prevent access
by an unauthorised person at all times,
except when it is necessary to open them to
carry out an essential operation in connection
with the poisons stored in them.
Penalty: 100 penalty units.
(2) This regulation applies to—
(a) a person referred to in Column 1 of Part 2 of
the table in regulation 5 as authorised to have
in his or her possession a Schedule 4 poison
or Schedule 8 poison; and
(b) an approved provider of an aged care service
if—
(i) in that service there is a resident who is
receiving a high level of residential
care; and
(ii) that resident has been supplied, on
prescription, with a Schedule 4 poison,
a Schedule 8 poison, or a Schedule 9
poison.
37. Additional security provisions required in certain
circumstances
(1) Subject to sub-regulation (2), the Secretary may—
(a) direct a person to whom regulation 34, 35
or 36 applies to provide more secure storage
for Schedule 4 poisons, Schedule 8 poisons
or Schedule 9 poisons than that described in
regulations 34, 35 and 36; or
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(b) grant approval for a person to store
substances other than Schedule 8 poisons or
Schedule 9 poisons in the same storage
facility as Schedule 8 poisons or Schedule 9
poisons.
(2) Before giving a direction or granting approval
under sub-regulation (1) the Secretary—
(a) must have regard to—
(i) the nature and quantity of the poisons
or controlled substances being stored;
and
(ii) the location, layout and construction of
the storage facility and the premises;
and
(iii) the warning devices and detectors with
which the storage facility and premises
are equipped; and
(iv) the number and frequency of
transactions; and
(v) the number of persons requiring access;
and
(b) may have regard to any other factors the
Secretary considers relevant in the
circumstances.
(3) A person who is directed by the Secretary to
provide more secure storage under sub-
regulation (1)(a) must provide that secure storage.
Penalty: 100 penalty units.
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Division 5—Records
38. Definition of transaction
In this Division "transaction" means the
manufacture, preparation, use, transfer within and
between premises, administration, sale, supply,
disposal or destruction of a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison.
39. Persons required to keep records
The following persons are required to keep
records under this Division—
(a) a registered medical practitioner, pharmacist,
veterinary practitioner, dentist, nurse
practitioner and authorised optometrist; and
(b) a person holding a licence, permit or warrant
to manufacture, sell, supply, purchase or
otherwise obtain, possess, administer or use
a Schedule 4 poison, Schedule 8 poison or
Schedule 9 poison; and
(c) a nurse authorised under regulation 5(2) to
be in possession of a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison; and
(d) an approved provider of an aged care service
if—
(i) in that service there is a resident who is
receiving a high level of residential
care; and
(ii) that resident has been supplied, on
prescription, with a Schedule 4 poison,
a Schedule 8 poison, or a Schedule 9
poison; and
(e) a person referred to in Column 1 of Part 2 of
the table in regulation 5 as authorised to have
in his or her possession a Schedule 4 poison
or Schedule 8 poison.
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40. Details to be contained in records
(1) A person required to keep records under this
Division must, as soon as practicable after
completing a transaction, record—
(a) the date of each transaction; and
(b) the name, form, strength and quantity of the
poison or controlled substance; and
(c) in the case of a transaction involving supply
on a prescription—
(i) the name of the prescriber; and
(ii) the directions for use as set out on the
prescription; and
(d) the name and address or location of persons
to whom the poison or controlled substance
is transferred, supplied, administered or
otherwise disposed of; and
(e) in the case of a Schedule 8 poison or
Schedule 9 poison purchased or obtained, the
name and address of the person from whom
the poison was purchased or obtained; and
(f) in the case of a Schedule 8 poison or
Schedule 9 poison which has been destroyed
by a registered medical practitioner,
pharmacist, veterinary practitioner or dentist
in accordance with regulation 51(3)(a), the
details set out in regulation 51(3)(b); and
(g) in the case of a Schedule 8 poison which has
been destroyed by a nurse practitioner in
accordance with regulation 51(2)(a), the
details set out in regulation 51(2)(b); and
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(h) in the case of the unused contents of a
previously sterile container containing a
Schedule 8 poison or a Schedule 9 poison
that are not required for administration to a
patient which has been destroyed by a
registered medical practitioner, pharmacist,
veterinary practitioner, dentist or nurse in
accordance with regulation 51(4)(a), the
details set out in regulation 51(4)(b); and
(i) in the case of a transaction involving supply
or administration to a specific person, the
name of the person carrying out the
transaction.
Penalty: 50 penalty units.
(2) Despite sub-regulation (1), a registered medical
practitioner, pharmacist, veterinary practitioner,
dentist, nurse practitioner or authorised
optometrist is not required to keep a record of the
destruction of Schedule 4 poisons.
41. Methods by which records are to be retained and
retrieved
(1) A person required to keep records under this
Division must ensure that the records of all
transactions in Schedule 8 poisons or Schedule 9
poisons kept by the person—
(a) are able to be readily sorted by poison or
controlled substance; and
(b) show the true and accurate balance of each
Schedule 8 poison and Schedule 9 poison
remaining in the person's possession after
each transaction; and
(c) show the name of the person carrying out the
transaction.
Penalty: 50 penalty units.
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(2) A person required to keep records under this
Division must keep records made by the person
readily retrievable in English.
Penalty: 50 penalty units.
(3) A person required to keep records under this
Division must retain a record of each transaction
in a Schedule 4 poison, Schedule 8 poison or
Schedule 9 poison in a readily retrievable form for
3 years from the date of the transaction.
Penalty: 50 penalty units.
(4) A person required to keep records under this
Division must produce on demand to an
authorised officer all records required to be kept
under this Division.
Penalty: 50 penalty units.
(5) A person required to keep records under this
Division must maintain the records made by him
or her of transactions in Schedule 8 poisons or
Schedule 9 poisons in a manner that ensures that
the records cannot be altered, obliterated, deleted
or removed without detection.
Penalty: 50 penalty units.
(6) An approved provider of an aged care service
where there is a resident who is receiving a high
level of residential care who has been supplied, on
prescription, with a Schedule 4 poison, Schedule 8
poison or Schedule 9 poison need not comply with
sub-regulation (1) in relation to Schedule 8
poisons or Schedule 9 poisons that are—
(a) supplied on prescription for a specific
person; and
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(b) supplied in tamper-evident compartments of
dose administration containers; and
(c) labelled by a registered medical practitioner,
pharmacist, dentist or nurse practitioner for
administration at times specified on the label.
42. Accurate records to be kept
A person required to keep records under this
Division must not knowingly make or cause to be
made an entry which is false or misleading in any
records in respect of a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison.
Penalty: 50 penalty units.
43. Discrepancies in records to be investigated
A person required to keep records under this
Division must—
(a) investigate without delay any discrepancies
found in the transaction records kept by that
person; and
(b) after that investigation, notify the Secretary
without delay of any discrepancy which
remains.
Penalty: 50 penalty units.
44. Lost or stolen records to be reported
A person required to keep records under this
Division must notify the Secretary without delay
of the circumstances of any loss, destruction or
theft of records kept by the person relating to
Schedule 4 poisons, Schedule 8 poisons or
Schedule 9 poisons.
Penalty: 50 penalty units.
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Division 6—Administration
45. Use of drugs and poisons restricted to person or
animal for whom they were supplied
(1) A person must not administer or use a Schedule 4
poison, Schedule 8 poison or Schedule 9 poison
supplied by a registered medical practitioner,
pharmacist, veterinary practitioner or dentist for
the treatment of a specific person or animal other
than for the treatment of that person or animal.
Penalty: 100 penalty units.
(2) A person must not administer or use a Schedule 4
poison or Schedule 8 poison supplied by a nurse
practitioner for the treatment of a specific person
other than for the treatment of that person.
Penalty: 100 penalty units.
(3) A person must not administer or use a Schedule 4
poison supplied by an authorised optometrist for
the treatment of a specific person other than for
the treatment of that person.
Penalty: 100 penalty units.
46. Administration of drugs and poisons to be
authorised
(1) A registered medical practitioner or dentist who
orders the administration of a Schedule 4 poison,
Schedule 8 poison or Schedule 9 poison to a
person—
(a) must provide that instruction in writing in a
legible and durable form; and
(b) must date and confirm that order with his or
her signature.
Penalty: 100 penalty units.
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(2) A nurse practitioner who orders the administration
of a Schedule 4 poison or Schedule 8 poison to a
person—
(a) must provide that instruction in writing in a
legible and durable form; and
(b) must date and confirm that order with his or
her signature.
Penalty: 100 penalty units.
(3) An authorised optometrist who orders the
administration of a Schedule 4 poison to a
person—
(a) must provide that instruction in writing in a
legible and durable form; and
(b) must date and confirm that order with his or
her signature.
Penalty: 100 penalty units.
(4) A person must not administer a Schedule 4
poison, Schedule 8 poison or Schedule 9 poison to
another person on the instruction of a registered
medical practitioner or dentist if—
(a) in the case of a Schedule 4 poison, it is more
than 12 months after the date on which the
instruction was given; or
(b) in the case of a Schedule 8 poison or
Schedule 9 poison, it is more than 6 months
after the date on which the instruction was
given.
Penalty: 100 penalty units.
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(5) A person must not administer a Schedule 4 poison
or Schedule 8 poison to another person on the
instruction of a nurse practitioner if—
(a) in the case of a Schedule 4 poison, it is more
than 12 months after the date on which the
instruction was given; or
(b) in the case of Schedule 8 poison, it is more
than 6 months after the date on which the
instruction was given.
Penalty: 100 penalty units.
(6) A person must not administer a Schedule 4 poison
to another person on the instruction of an
authorised optometrist if it is more than 12 months
after the date on which the instruction was given.
Penalty: 100 penalty units.
(7) A person referred to in Column 1 of Part 2 of the
table in regulation 5 must not administer a
Schedule 4 poison or Schedule 8 poison other than
to the extent authorised by Column 2 of Part 2 of
the Table.
Penalty: 100 penalty units.
47. Administration of drugs and poisons by a nurse
(1) A nurse must not administer a Schedule 9 poison
to a person other than—
(a) in accordance with the directions for use on
the container of the Schedule 9 poison
supplied by a registered medical practitioner,
pharmacist or dentist; or
(b) on the written instruction of a registered
medical practitioner or dentist; or
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(c) on the oral instructions of a registered
medical practitioner or dentist to the nurse if,
in the opinion of the registered medical
practitioner or dentist, an emergency exists;
or
(d) on the written transcription of the oral
instructions referred to in paragraph (c) by
another nurse who received those
instructions; or
(e) in accordance with regulation 5(2) or an
approval of the Secretary under
regulation 5(3).
(2) A nurse must not administer a Schedule 8 poison
other than—
(a) in accordance with the directions for use on
the container of the Schedule 8 poison
supplied by a registered medical practitioner,
pharmacist, dentist or nurse practitioner; or
(b) on the written instruction of a registered
medical practitioner, dentist or nurse
practitioner; or
(c) on the oral instructions of a registered
medical practitioner, dentist or nurse
practitioner to the nurse if, in the opinion of
the registered medical practitioner, dentist or
nurse practitioner, an emergency exists; or
(d) on the written transcription of the oral
instructions referred to in paragraph (c) by
another nurse who received those
instructions; or
(e) in accordance with regulation 5(2) or an
approval of the Secretary under
regulation 5(3).
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(3) A nurse must not administer a Schedule 4 poison
other than—
(a) in accordance with the directions for use on
the container of the Schedule 4 poison
supplied by a registered medical practitioner,
pharmacist, dentist, nurse practitioner or
authorised optometrist; or
(b) on the written instruction of a registered
medical practitioner, dentist, nurse
practitioner or authorised optometrist; or
(c) on the oral instructions of a registered
medical practitioner, dentist, nurse
practitioner or authorised optometrist to the
nurse, if in the opinion of the registered
medical practitioner, dentist, nurse
practitioner or authorised optometrist, an
emergency exists; or
(d) on the written transcription of the oral
instructions referred to in paragraph (c) by
another nurse who received those
instructions; or
(e) in accordance with regulation 5(2) or an
approval of the Secretary under
regulation 5(3).
Penalty: 100 penalty units.
(4) A registered medical practitioner, dentist, nurse
practitioner or authorised optometrist who issues
oral instructions in accordance with sub-
regulation (1)(c), (2)(c) or (3)(c) (as the case
requires) must as soon as practicable—
(a) confirm those oral instructions in writing;
and
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(b) include them or provide them for inclusion in
the treatment records of the person
concerned.
Penalty: 100 penalty units.
48. Self-administration of drugs and poisons restricted
A person must not use, prescribe, sell or supply a
Schedule 4 poison, a Schedule 8 poison or a
Schedule 9 poison (as the case requires) for the
purpose of self-administration unless the person—
(a) in the case of a Schedule 9 poison—
(i) is a patient for whom a registered
medical practitioner or dentist has
prescribed that poison; and
(ii) is not the registered medical
practitioner or dentist who prescribed
that poison; and
(b) in the case of a Schedule 8 poison—
(i) is a patient for whom a registered
medical practitioner, dentist or nurse
practitioner has prescribed that poison;
and
(ii) is not the registered medical
practitioner, dentist or nurse
practitioner who prescribed that
poison; and
(c) in the case of a Schedule 4 poison—
(i) is a patient for whom a registered
medical practitioner, dentist, nurse
practitioner or authorised optometrist
(in accordance with the endorsement of
his or her registration) has prescribed
that poison; and
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(ii) is not the registered medical
practitioner, dentist, nurse practitioner
or authorised optometrist who
prescribed that poison; and
(d) in any case, uses that poison to the extent
and for the purpose for which it was
prescribed, sold or supplied.
Penalty: 100 penalty units.
49. Administration or supply of drugs and poisons
prohibited if to support drug dependency
A person must not administer, prescribe, sell or
supply a drug of dependence or a Schedule 4
poison, Schedule 8 poison or Schedule 9 poison to
any person merely for the purpose of supporting
the drug dependence of that person.
Penalty: 100 penalty units.
Division 7—Destruction of Schedule 8 Poisons and
Schedule 9 Poisons
50. Wilful destruction prohibited
Subject to this Division, a person must not
wilfully destroy a Schedule 8 poison or
Schedule 9 poison.
Penalty: 100 penalty units.
51. Exceptions
(1) Regulation 50 does not apply to—
(a) a Schedule 8 poison or Schedule 9 poison
destroyed by or under the supervision of an
authorised officer; or
(b) a Schedule 8 poison or Schedule 9 poison for
which a court order has been granted for its
destruction; or
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(c) a Schedule 8 poison or Schedule 9 poison
which has been taken into possession by a
member of the police force and for which an
order for destruction has been issued by an
officer of rank not below that of Inspector of
the Victoria Police; or
(d) a narcotic plant or seed of any narcotic plant
as defined in section 70 of the Act.
(2) Subject to sub-regulation (5), regulation 50 does
not apply to a Schedule 8 poison if—
(a) it is destroyed by a nurse practitioner in the
presence of another person who is a
registered medical practitioner, pharmacist,
veterinary practitioner, dentist or nurse; and
(b) the details of the destruction are recorded in
the records required to be kept under
regulation 40, including—
(i) the name, strength and quantity of the
poisons or controlled substances
destroyed; and
(ii) the method and place of destruction;
and
(iii) the names of the persons carrying out
the destruction; and
(iv) the names of the witnesses.
(3) Subject to sub-regulation (5), regulation 50 does
not apply to a Schedule 8 poison or Schedule 9
poison if—
(a) it is destroyed by a registered medical
practitioner, pharmacist, veterinary
practitioner or dentist in the presence of
another person who is a registered medical
practitioner, pharmacist, veterinary
practitioner, dentist or nurse; and
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(b) the details of the destruction are recorded in
the records required to be kept under
regulation 40, including—
(i) the name, strength and quantity of the
poisons or controlled substances
destroyed; and
(ii) the method and place of destruction;
and
(iii) the names of the persons carrying out
the destruction; and
(iv) the names of the witnesses.
(4) Subject to sub-regulation (5), regulation 50 does
not apply to the unused contents of a previously
sterile container containing a Schedule 8 poison or
a Schedule 9 poison that are not required for
administration to a patient if—
(a) those contents are destroyed by a registered
medical practitioner, pharmacist, veterinary
practitioner, dentist or nurse; and
(b) the details of the destruction are recorded in
the records required to be kept under
regulation 40, including—
(i) the name, strength and quantity of the
poisons or controlled substances
destroyed; and
(ii) the method and place of destruction;
and
(iii) the name of the person carrying out the
destruction.
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(5) The Secretary may direct a person referred to in
sub-regulation (2), (3) or (4) to comply with any
requirements relating to the destruction of a
Schedule 8 poison or Schedule 9 poison (as the
case requires) specified in writing by the
Secretary.
Division 8—Cultivation of Narcotic Plants
52. Authority to cultivate narcotic plants for non-
therapeutic uses
For the purposes of section 72 of the Act, the
Secretary may, in his or her discretion, authorise
in writing a fit and proper person to cultivate a
narcotic plant as defined in section 70 of the Act
for a use other than a therapeutic use.
Division 9—Warrants for Ovulatory Stimulants,
Prostaglandins, Retinoids and Thalidomide
53. Requirement for warrants
(1) A registered medical practitioner must not
purchase, obtain, use, supply or prescribe an
ovulatory stimulant, a prostaglandin, a retinoid or
thalidomide unless he or she holds a warrant
under the Act to do so.
Penalty: 100 penalty units.
(2) Despite sub-regulation (1), a registered medical
practitioner acting in accordance with the
instruction of a registered medical practitioner
who holds a warrant may use, supply or prescribe
an ovulatory stimulant, a prostaglandin, a retinoid
or thalidomide with respect to a specific patient in
accordance with the authorisation given by the
warrant.
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54. Warrant number to be included in any prescription
(1) A registered medical practitioner who prescribes
an ovulatory stimulant, a prostaglandin, a retinoid
or thalidomide must include the warrant number
on the prescription.
Penalty: 10 penalty units.
(2) A registered medical practitioner who prescribes
an ovulatory stimulant, a prostaglandin, a retinoid
or thalidomide on the direction of the warrant
holder must include on the prescription the name
of the registered medical practitioner who holds
the warrant.
Penalty: 10 penalty units.
55. Prohibition on dentists
A dentist must not purchase, obtain, use, supply or
prescribe an ovulatory stimulant, a prostaglandin,
a retinoid or thalidomide.
Penalty: 100 penalty units.
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PART 3—PRESCRIBED POISONS FOR CATEGORIES OF
NURSE PRACTITIONER
56. Prescribed poisons related to certain categories of
nurse practitioner
(1) The prescribed Schedule 2 poisons, Schedule 3
poisons, Schedule 4 poisons and Schedule 8
poisons that a nurse practitioner whose
registration is endorsed with the category of nurse
practitioner—wound management is authorised to
obtain and have in his or her possession and to
use, sell or supply are the poisons set out in Part 1
of Schedule 3 to these Regulations.
(2) The prescribed Schedule 3 poisons and Schedule 4
poisons that a nurse practitioner whose
registration is endorsed with the category of nurse
practitioner—intensive care unit liaison is
authorised to obtain and have in his or her
possession and to use, sell or supply are the
poisons set out in Part 2 of Schedule 3 to these
Regulations.
(3) The prescribed Schedule 3 poisons and Schedule 4
poisons that a nurse practitioner whose
registration is endorsed with the category of nurse
practitioner—young people's health is authorised
to obtain and have in his or her possession and to
use, sell or supply are the poisons set out in Part 3
of Schedule 3 to these Regulations.
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(4) The prescribed Schedule 2 poisons, Schedule 3
poisons, Schedule 4 poisons and Schedule 8
poisons that a nurse practitioner whose
registration is endorsed with the category of nurse
practitioner—palliative care is authorised to
obtain and have in his or her possession and to
use, sell or supply are the poisons set out in Part 4
of Schedule 3 to these Regulations.
__________________
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PART 4—SCHEDULE 3 POISONS
57. Therapeutic need to be determined—registered
medical practitioners
A registered medical practitioner must not
administer, prescribe, sell or supply a Schedule 3
poison unless—
(a) that poison is for the medical treatment of a
person under his or her care; and
(b) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that
poison.
Penalty: 50 penalty units.
58. Therapeutic need to be determined—nurse
practitioners
A nurse practitioner must not administer,
prescribe, sell or supply a Schedule 3 poison
unless—
(a) that poison is for the treatment of a person
under his or her care; and
(b) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that
poison.
Penalty: 50 penalty units.
59. Therapeutic need to be determined—veterinary
practitioners
A veterinary practitioner must not administer,
prescribe, sell or supply a Schedule 3 poison
unless—
(a) that poison is for the treatment of an animal
under his or her care; and
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(b) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that
poison.
Penalty: 50 penalty units.
60. Therapeutic need to be determined—dentists
A dentist must not administer, prescribe, sell or
supply a Schedule 3 poison unless—
(a) that poison is for the dental treatment of a
person under his or her care; and
(b) he or she has taken all reasonable steps to
ensure a therapeutic need exists for that
poison.
Penalty: 50 penalty units.
61. Therapeutic need to be determined—pharmacists
A pharmacist who supplies a Schedule 3 poison
other than—
(a) by wholesale; or
(b) on the prescription of a registered medical
practitioner, nurse practitioner, dentist or
veterinary practitioner—
must do so only for the therapeutic use of a person
or animal, after having taken all reasonable steps
to ensure a therapeutic need exists for that poison.
Penalty: 50 penalty units.
62. Restrictions on storage and display
A person who is authorised or licensed under the
Act to sell or supply Schedule 3 poisons must not
keep, store or display any Schedule 3 poison—
(a) in a manner which readily allows self-
selection by the public; or
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(b) in a manner which will promote the sale of
that Schedule 3 poison or draw undue
attention to it.
Penalty: 50 penalty units.
63. Requirements to supply
(1) A registered medical practitioner, pharmacist,
veterinary practitioner, dentist or nurse
practitioner who sells or supplies a Schedule 3
poison to a person must—
(a) personally deliver or personally supervise its
delivery to the person; and
(b) provide directions for the use of the
Schedule 3 poison; and
(c) place a label on the container which uniquely
identifies the supplier.
Penalty: 50 penalty units.
(2) Sub-regulation (1) does not apply to a pharmacist
who sells or supplies a Schedule 3 poison by
wholesale.
(3) Sub-regulations (1)(a) and (b) do not apply to a
pharmacist who sells or supplies a Schedule 3
poison on the prescription of a registered medical
practitioner, veterinary practitioner, dentist or
nurse practitioner.
64. Administration or supply prohibited if to support
drug dependency
A person must not administer, prescribe, sell or
supply a Schedule 3 poison to a person merely for
the purpose of supporting the drug dependence of
that person.
Penalty: 50 penalty units.
__________________
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Part 5—Schedule 7 Poisons
Drugs, Poisons and Controlled Substances Regulations 2006
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63
PART 5—SCHEDULE 7 POISONS
65. Controls concerning listed regulated poisons
A person must not manufacture, sell, supply,
purchase or otherwise obtain, possess or use a
listed regulated poison unless the person is
authorised, licensed or permitted under the Act or
these Regulations to do so.
Penalty: 100 penalty units.
66. Storage requirements
A person who sells or supplies any Schedule 7
poison by retail in accordance with the Act
(whether or not by authority under section 13 of
the Act) must store all Schedule 7 poisons in that
person's possession in a storage facility which is
not accessible to the public, unless access to that
area or facility is under the personal supervision
of that person or a person acting under his or her
direction.
Penalty: 50 penalty units.
67. Licences, permits or warrants required for special
Schedule 7 substances
A person must not possess or use a special
Schedule 7 substance unless he or she holds a
licence, permit or warrant issued under the Act.
Penalty: 100 penalty units.
__________________
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PART 6—GENERAL REQUIREMENTS
68. Poisons to be sold by wholesale and retail in original
unopened packs
(1) A person who sells or supplies a poison or
controlled substance by wholesale or retail must
sell or supply that poison or controlled substance
only in the original unopened pack as received
from the person who supplied that wholesaler or
retailer.
Penalty: 50 penalty units.
(2) Sub-regulation (1) does not apply to the sale or
supply of a poison or controlled substance in the
course of his or her professional practice by a
person authorised under section 13(1) of the Act
with respect to that poison or controlled
substance.
69. Transfer of poisons to inappropriate containers
prohibited
Except in the course of actual use of a poison or
controlled substance, a person must not remove
that poison or controlled substance from the
container in which it was dispensed, sold or
supplied to put that poison or controlled
substance—
(a) into an unlabelled receptacle or container; or
(b) into a receptacle or container which does not
accurately identify that poison or controlled
substance.
Penalty: 50 penalty units.
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70. Lost or stolen poisons to be notified
(1) A person to whom this regulation applies who
loses a poison or controlled substance or from
whom a poison or controlled substance is stolen
must immediately upon becoming aware of that
loss or theft notify the Secretary or a member of
the Victoria Police of the loss or theft.
Penalty: 20 penalty units.
(2) This regulation applies to—
(a) a registered medical practitioner, pharmacist,
veterinary practitioner, dentist, nurse
practitioner and an authorised optometrist; or
(b) a person who holds a licence, permit or
warrant issued under the Act or these
Regulations; or
(c) a person who is referred to in Column 1 of
Part 2 of the table in regulation 5; or
(d) a person who sells or supplies any
Schedule 7 poison by retail; or
(e) a person who is an approved provider of an
aged care service if—
(i) in that service, there is a resident who is
receiving a high level of residential
care; and
(ii) that resident has been supplied, on
prescription, with a Schedule 4 poison,
Schedule 8 poison or Schedule 9
poison.
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71. Access to certain poisons restricted to a needs basis
A person who is authorised by, or licensed or
permitted under, the Act or the regulations, to be
in possession of a Schedule 4 poison, listed
regulated poison, Schedule 8 poison or Schedule 9
poison must take all reasonable steps to restrict
access to that poison or controlled substance to—
(a) persons who are authorised by, or licensed or
permitted under the Act or the regulations, to
be in possession of that poison or controlled
substance; and
(b) persons to whom access is required for
carrying out essential operations in relation
to that poison or controlled substance.
Penalty: 100 penalty units.
72. Form of seizure notice under section 43(1) of the Act
For the purposes of section 43(1) of the Act, the
prescribed form is the form of DP4 in Schedule 2.
73. Form of complaint notice against a seizure under
section 43(2) of the Act
For the purposes of section 43(2) of the Act, the
prescribed form is the form of DP5 in Schedule 2.
__________________
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Part 7—Licences and Permits Issued under the Act
Drugs, Poisons and Controlled Substances Regulations 2006
S.R. No. 57/2006
67
PART 7—LICENCES AND PERMITS ISSUED UNDER
THE ACT
74. Licence to sell or supply Schedule 2 poisons by retail
The Secretary must not grant to a person a licence
under the Act to sell or supply by retail a
Schedule 2 poison unless the business premises of
that person are situated at least 25 kilometres
distance away by the shortest practicable road
from the nearest pharmacy business.
75. Fees
(1) The prescribed fee for the issue of a licence or
permit specified in an item in Column 1 of the
following table is the amount specified in
Column 2 of that table in respect of that licence or
permit.
(2) The prescribed fee for an amendment of a licence
or permit specified in an item in Column 1 of the
table, where the amendment requires inspection of
the premises by an authorised officer, is the
amount specified in Column 3 of that table in
respect of that licence or permit.
(3) The prescribed fee for the renewal of a licence or
permit specified in an item in Column 1 of the
table is the amount specified in Column 4 of that
table in respect of that licence or permit.
(4) The prescribed fee for an amendment of a licence
or permit which does not require the inspection of
premises by an authorised officer is 5⋅3 fee units.
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TABLE
Column 1
Description of licence
or permit
Column 2
Issue of
licence or
permit
Column 3
Amendment of
licence or
permit where
amendment
requires
inspection of
premises by an
authorised
officer
Column 4
Renewal of
licence or
permit
1. A licence to
manufacture and
sell or supply by
wholesale any
Schedule 8 poison
or Schedule 9
poison other than
heroin.
107⋅6 fee
units
107⋅6 fee units 73⋅8 fee units
2. Subject to item 3,
a licence to
manufacture and
sell or supply by
wholesale any
Schedule 4 poison
(alone or together
with any
Schedule 2
poison,
Schedule 3 poison
or Schedule 7
poison or any
combination of
those poisons).
78⋅8 fee units 78⋅8 fee units 38⋅6 fee units
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Column 1
Description of licence
or permit
Column 2
Issue of
licence or
permit
Column 3
Amendment of
licence or
permit where
amendment
requires
inspection of
premises by an
authorised
officer
Column 4
Renewal of
licence or
permit
3. A licence to
manufacture and
sell or supply by
wholesale any
Schedule 2 poison,
Schedule 3 poison
or Schedule 7
poison or any
combination of
those poisons.
56⋅9 fee units 56⋅9 fee units 20⋅1 fee units
4. A licence to
manufacture and
sell or supply by
retail a Schedule 7
poison (other than
a listed regulated
poison).
49⋅3 fee units 49⋅3 fee units 18⋅6 fee units
5. Subject to item 6,
a licence to sell or
supply by
wholesale any
Schedule 8 poison
or Schedule 9
poison other than
heroin.
107⋅6 fee
units
107⋅6 fee units 73⋅8 fee units
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Column 1
Description of licence
or permit
Column 2
Issue of
licence or
permit
Column 3
Amendment of
licence or
permit where
amendment
requires
inspection of
premises by an
authorised
officer
Column 4
Renewal of
licence or
permit
6. A licence to sell or
supply by
wholesale by
Indent any
Schedule 8 poison
or Schedule 9
poison other than
heroin.
49⋅3 fee units 49⋅3 fee units 33⋅4 fee units
7. Subject to item 8,
a licence to sell or
supply by
wholesale any
Schedule 4 poison
(alone or together
with any
Schedule 2 poison,
Schedule 3 poison
or Schedule 7
poison or any
combination of
those poisons).
78⋅8 fee units 78⋅8 fee units 38⋅6 fee units
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Column 1
Description of licence
or permit
Column 2
Issue of
licence or
permit
Column 3
Amendment of
licence or
permit where
amendment
requires
inspection of
premises by an
authorised
officer
Column 4
Renewal of
licence or
permit
8. A licence to sell or
supply by
wholesale by
Indent any
Schedule 4 poison
(alone or together
with any
Schedule 2 poison,
Schedule 3 poison
or Schedule 7
poison or any
combination of
those poisons).
49⋅3 fee units 49⋅3 fee units 22⋅7 fee units
9. Subject to item 10,
a licence to sell or
supply by
wholesale any
Schedule 2 poison,
Schedule 3 poison
or Schedule 7
poison or any
combination of
those poisons.
56⋅9 fee units 56⋅9 fee units 20⋅1 fee units
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Column 1
Description of licence
or permit
Column 2
Issue of
licence or
permit
Column 3
Amendment of
licence or
permit where
amendment
requires
inspection of
premises by an
authorised
officer
Column 4
Renewal of
licence or
permit
10. A licence to sell or
supply by
wholesale by
Indent any
Schedule 2 poison,
Schedule 3 poison
or Schedule 7
poison or any
combination of
those poisons.
49⋅3 fee units 49⋅3 fee units 18⋅6 fee
units
11. A licence to sell or
supply by retail
any Schedule 2
poison.
33⋅7 fee units 33⋅7 fee units 14⋅1 fee
units
12. A permit to
purchase or obtain
and use for
industrial,
educational,
advisory or
research purposes
any Schedule 8
poison or
Schedule 9 poison
(alone or together
with any
Schedule 2 poison,
Schedule 3 poison,
Schedule 4 poison
or Schedule 7
poison or any
combination of
those poisons).
47⋅8 fee units 47⋅8 fee units 18⋅3 fee
units
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Column 1
Description of licence
or permit
Column 2
Issue of
licence or
permit
Column 3
Amendment of
licence or
permit where
amendment
requires
inspection of
premises by an
authorised
officer
Column 4
Renewal of
licence or
permit
13. A permit to
purchase or obtain
and use for
industrial,
educational,
advisory or
research purposes
any Schedule 2
poison, Schedule 3
poison, Schedule 4
poison or
Schedule 7 poison
or any combination
of those poisons.
43⋅8 fee units 43⋅8 fee units 15⋅5 fee
units
14. A permit to
purchase or obtain
and use any poison
or controlled
substance for the
provision of health
services by the
following types of
health service
provider—
Type A (single
site with no
beds);
36⋅2 fee units 36⋅2 fee units 14⋅4 fee
units
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Column 1
Description of licence
or permit
Column 2
Issue of
licence or
permit
Column 3
Amendment of
licence or
permit where
amendment
requires
inspection of
premises by
an authorised
officer
Column 4
Renewal of
licence or
permit
Type B
(residential aged
care with single
storage facility
(no bed limit) or
single site with
1 to 30 beds);
55⋅5 fee units 55⋅5 fee units 20⋅5 fee units
Type C (multiple
sites with no
beds or single
site with 31 to
100 beds);
76⋅3 fee units 76⋅3 fee units 34⋅2 fee units
Type D (multiple
sites or single
site with more
than 100 beds).
108⋅2 fee
units
108⋅2 fee units 48⋅3 fee units
__________________
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PART 8—TRANSITIONALS
76. Continuity of approvals, authorisations and
directions
(1) An approval given by the Secretary under
regulations 5(2)(a) and 5(2)(b) of the Drugs,
Poisons and Controlled Substances Regulations
1995 and in force immediately before the
commencement of these Regulations continues in
force as if that approval had been given under
regulation 6 of these Regulations.
(2) An approval given by the Secretary under
regulation 5(4) of the Drugs, Poisons and
Controlled Substances Regulations 1995 and in
force immediately before the commencement of
these Regulations continues in force as if that
approval had been given under regulation 5(3) of
these Regulations.
(3) An approval given by the Secretary under
regulation 23(1) of the Drugs, Poisons and
Controlled Substances Regulations 1995 and in
force immediately before the commencement of
these Regulations continues in force as if that
approval had been given under regulation 26(1) of
these Regulations.
(4) A direction given by the Secretary under
regulation 36(1) of the Drugs, Poisons and
Controlled Substances Regulations 1995 and in
force immediately before the commencement of
these Regulations continues in force as if that
direction had been given under regulation 37(1)(a)
of these Regulations.
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(5) A direction given by the Secretary under
regulation 50(2) of the Drugs, Poisons and
Controlled Substances Regulations 1995 and in
force immediately before the commencement of
these Regulations continues in force as if that
direction had been given under regulation 51(5) of
these Regulations.
(6) An authorisation given by the Secretary under
regulation 51 of the Drugs, Poisons and
Controlled Substances Regulations 1995 and in
force immediately before the commencement of
these Regulations continues in force as if that
authorisation had been given under regulation 52
of these Regulations.
__________________
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SCHEDULES
SCHEDULE 1
REVOKED STATUTORY RULES
S.R. No. Title
20/1996 Drugs, Poisons and Controlled Substances (Amendment)
Regulations 1996
47/1996 Drugs, Poisons and Controlled Substances (Further
Amendment) Regulations 1996
81/1996 Drugs, Poisons and Controlled Substances (Labelling and
Container) (Amendment) Regulations 1996
26/1997 Drugs, Poisons and Controlled Substances (Fees) Regulations
1997
75/1997 Drugs, Poisons and Controlled Substances (Amendment)
Regulations 1997
132/1998 Drugs, Poisons and Controlled Substances (Optometrists)
Regulations 1998
159/1998 Drugs, Poisons and Controlled Substances (Amendment)
Regulations 1998
86/2002 Drugs, Poisons and Controlled Substances (Fees) Regulations
2002
67/2003 Drugs, Poisons and Controlled Substances (Fees) Regulations
2003
43/2004 Drugs, Poisons and Controlled Substances (Amendment)
Regulations 2004
44/2004 Drugs, Poisons and Controlled Substances (Division 2 Nurses
Amendment) Regulations 2004
150/2004 Drugs, Poisons and Controlled Substances (Nurse Practitioner
and Miscellaneous Amendments) Regulations 2004
39/2005 Drugs, Poisons and Controlled Substances (Amendment)
Regulations 2005
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S.R. No. Title
117/2005 Drugs, Poisons and Controlled Substances (Fees) Regulations
2005
16/2006 Drugs, Poisons and Controlled Substances (Amendment)
(Nurse Practitioners - Palliative Care) Regulations 2006
__________________
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SCHEDULE 2
FORMS
Regulation 18
FORM DP1
Drugs, Poisons and Controlled Substances Regulations 2006
NOTIFICATION OF DRUG DEPENDENT PERSON
I, [full name of registered medical practitioner/nurse practitioner] of
[address of registered medical practitioner/nurse practitioner—including
telephone and fax numbers]
have reason to believe that [full name of patient] of [address of patient] is
dependent on [name of drug(s)] and my belief is based on the following
grounds:
PATIENT DETAILS
Aliases (if any) Height
Occupation Colour of eyes
Sex Tattoos
Date of birth Other distinguishing features
Mother's full maiden name Other drugs used by patient
Marital status Approximate period of drug dependency
Intention to prescribe Source of drugs
DPU number (if known)
Signature of registered medical
practitioner/nurse practitioner
Date
_______________
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FORM DP2
Regulations 19, 21(3), 22(3)
Drugs, Poisons and Controlled Substances Regulations 2006
TREATMENT WITH SCHEDULE 8 POISONS OR SCHEDULE 9
POISONS BY A REGISTERED MEDICAL PRACTITIONER OR
SCHEDULE 8 POISONS BY A NURSE PRACTITIONER
(Notice of and application for permit to administer, prescribe or supply)
PART A: FOR TREATMENT WITH SCHEDULE 8 OR SCHEDULE 9
POISONS OTHER THAN METHADONE OR BUPRENORPHINE
Section 1: (To be completed in all cases)
Full name of patient Date of birth Sex
Private address of patient Postcode
Full name and qualifications of registered medical practitioner/nurse
practitioner
Address of registered medical practitioner/nurse
practitioner
Postcode
Telephone and fax no. of registered medical practitioner/nurse practitioner
Name and address of hospital where patient is undergoing treatment
(if applicable)
Clinical diagnosis
Section 2: (To be completed if the patient requires continuing treatment)
Schedule 8 poison(s) or Schedule 9 poison(s)* for which permit is requested:
NAME OF
POISON(S)
EXPECTED MAXIMUM DAILY DOSE
Duration for which that poison(s) has been used
Details of other treatment (if applicable)
I have/have not previously applied for a permit to administer, prescribe or
supply a Schedule 8 poison or a Schedule 9 poison* to this patient.
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Section 3: (Notification of specified conditions and circumstances as
required by section 35(2A) of the Drugs, Poisons and Controlled
Substances Act 1981)
Condition and circumstances
Schedule 8 drugs that may be necessary
Signature of registered medical practitioner/nurse
practitioner
Date
*References to Schedule 9 poisons must be deleted where this Form is
completed by a nurse practitioner
——
PART B: FOR TREATMENT OF AN OPIATE DEPENDENT
PERSON WITH METHADONE OR BUPRENORPHINE
I, [full name of registered medical practitioner/ nurse practitioner] of
[address of registered medical practitioner/nurse practitioner, including
postcode, phone and fax numbers] certify that this patient shows evidence of
dependence on an opioid drug and that, in my opinion,
methadone/buprenorphine is required in support of treatment.
Personal Details:
Full name of patient
Address of patient
Date of birth
DPU number (if known)
Sex
Aliases (if any)
Mother's full maiden name
Height
Medical Details of Patient:
Starting drug
Starting methadone/buprenorphine dose
Anticipated date of first dose
Period for which permit sought (if short term)
Has patient been on a methadone or buprenorphine
program previously? (Yes/No)
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If yes, details of contact with previous prescriber or dosing pharmacy
Is patient transferring from another prescriber? Yes/No
If Yes, indicate prescriber's name and suburb
Is that prescriber aware of transfer?
Last drug used by that prescriber? (methadone/buprenorphine)
Name, address and telephone number of person dispensing
methadone/buprenorphine
Signature of registered medical practitioner/nurse practitioner
Date
_______________
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FORM DP3
Regulation 20
Drugs, Poisons and Controlled Substances Regulations 2006
PERMIT TO ADMINISTER, PRESCRIBE OR SUPPLY A
SCHEDULE 8 POISON OR SCHEDULE 9 POISON BY A
REGISTERED MEDICAL PRACTITIONER OR A SCHEDULE 8
POISON BY A NURSE PRACTITIONER
This permit is granted to [full name and address of registered medical
practitioner/nurse practitioner]
and authorises that registered medical practitioner/nurse practitioner to
administer, prescribe or supply the following poison(s) in accordance with
the following details and conditions. The poison(s) must not be
administered, prescribed or supplied in excess of the quantities specified, or
for a period greater than that specified in this permit.
Name of patient
Address of patient
NAME OF POISON MAXIMUM DOSE
Special conditions: (if any)
This permit is valid from [date] to [date (if applicable)] unless sooner
revoked or suspended.
Date Secretary
_______________
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FORM DP4
Regulation 72
Drugs, Poisons and Controlled Substances Regulations 2006
NOTICE OF SEIZURE
To of
I, an authorised officer under the Drugs, Poisons and
Controlled Substances Act 1981 give notice that I have at a.m./p.m.
this day seized on the following grounds:
at
in the municipal district of the poisons or
controlled substances, other substances or documents described below:
of which you are
Unless you, or a person claiming the poisons or controlled substances, other
substances or documents complain to a registrar of the Magistrates' Court
within 96 hours of seizure by giving notice of complaint in the form of
Form DP5 to the Drugs, Poisons and Controlled Substances Regulations
2006, and a copy of that notice to the authorised officer who made the
seizure, the poisons or controlled substances, other substances or documents
will be destroyed or disposed of.
Dated at this day of 20 ,
at a.m./p.m.
Authorised Officer
Whose address for service of any notice of complaint verified by an
accompanying statutory declaration is
_______________
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FORM DP5
Regulation 73
Drugs, Poisons and Controlled Substances Regulations 2006
NOTICE OF COMPLAINT IN RESPECT OF A SEIZURE
To the registrar of the Magistrates' Court at
I, of
[Full name] [Address]
being claimant of the poisons or controlled substances, other substances or
documents described below—
which were seized by
on the day of at a.m./p.m., in accordance
with section 43(2) of the Drugs, Poisons and Controlled Substances Act
1981, complain about that seizure.
[Signature of complainant]
[Date]
Note:
Section 43(2) of the Drugs, Poisons and Controlled Substances Act 1981
requires that in lodging a notice of complaint to the registrar of the
Magistrates' Court—
(a) the notice must be verified by an accompanying statutory
declaration; and
(b) a copy of the notice and statutory declaration must be given to the
authorised officer who made the seizure.
__________________
Sch. 2
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SCHEDULE 3
Regulation 56
PART 1
NURSE PRACTITIONER—WOUND MANAGEMENT
The prescribed poisons that a nurse practitioner—wound management is
authorised to obtain and have in his or her possession and to use, sell or
supply are the substances listed below—
Schedule 2 poisons—
Codeine
Lignocaine
Paracetamol
Schedule 3 poisons—
Clotrimazole
Codeine
Iron compounds
Miconazole
Schedule 4 poisons—
Amoxycillin
Betamethasone
Bupivacaine
Cephalexin
Ciprofloxacin
Clavulanic acid
Clindamycin
Codeine
Dicloxacillin
Doxycycline
Flucloxacillin
Lignocaine
Methylprednisolone
Metronidazole
Mupirocin
Silver sulfadiazine
Terbinafine
Tramadol
Triamcinolone
Sch. 3
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Schedule 8 poisons—
Morphine
Oxycodone
PART 2
NURSE PRACTITIONER—INTENSIVE CARE UNIT LIAISON
The prescribed poisons that a nurse practitioner—intensive care unit liaison is
authorised to obtain and have in his or her possession and to use, sell or
supply are the substances listed below—
Schedule 3 poison—
Adrenaline
Schedule 4 poisons—
Adrenaline
Digoxin
Dobutamine
Dopamine
Frusemide
PART 3
NURSE PRACTITIONER—YOUNG PEOPLE'S HEALTH
The prescribed poisons that a nurse practitioner—young people's health is
authorised to obtain and have in his or her possession and to use, sell or
supply are the substances listed below—
Schedule 3 poisons—
Levonorgestrel
Salbutamol
Schedule 4 poisons—
Azithromycin
Ethinyloestradiol
Hepatitis B vaccine
Levonorgestrel
Medroxyprogesterone
Sch. 3
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PART 4
NURSE PRACTITIONER—PALLIATIVE CARE
The prescribed poisons that a nurse practitioner—palliative care is authorised
to obtain and have in his or her possession and to use, sell or supply are the
substances listed below—
Schedule 2 poisons—
Aspirin
Atropa Belladonna
Atropine Sulphate
Codeine
Hyoscine Butylbromide
Ibuprofen
Loperamide
Miconazole
Naproxen
Nystatin
Pholcodine
Ranitidine
Schedule 3 poisons—
Codeine
Diphenoxylate
Diclofenac
Macrogol 3350
Nystatin
Miconazole
Metoclopramide
Prochlorperazine
Schedule 4 poisons—
Amitriptyline
Amphotericin
Aspirin
Atropine
Atropa Belladonna
Carbamazepine
Clonazepam
Codeine
Dexamethasone
Diazepam
Diclofenac
Diphenoxylate
Domperidone
Gabapentin
Sch. 3
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Haloperidol
Hyoscine
Ibuprofen
Loperamide
Lorazepam
Metoclopramide
Metronidazole
Miconazole
Midazolam
Naproxen
Naloxone
Nitrazepam
Nystatin
Omeprazole
Pantoprazole
Paracetamol
Pholcodine
Prednisolone
Prochlorperazine
Ranitidine
Sodium Valproate
Temazepam
Tramadol
Schedule 8 poisons—
Codeine
Fentanyl
Hydromorphone
Morphine
Oxycodone
═══════════════
Sch. 3
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ENDNOTES
Fee Units
These Regulations provide for fees by reference to fee units established under
the Monetary Units Act 2004.
The amount of the fee is to be calculated, in accordance with section 7 of that
Act, by multiplying the number of fee units applicable by the value of a fee
unit.
The value of a fee unit for the financial year commencing 1 July 2005 is
$10.49. The value of a fee unit for the financial year commencing 1 July
2006 is $10.75. The amount of the calculated fee may be rounded to the
nearest 10 cents.
The value of a fee unit for future financial years is to be fixed by the
Treasurer under section 5 of the Monetary Units Act 2004. The value of a
fee unit for a financial year must be published in the Government Gazette and
a Victorian newspaper before 1 June in the preceding financial year.
——
Table of Applied, Adopted or Incorporated Matter Required by the
Subordinate Legislation Regulations 2004
Note that the following table of applied, adopted or incorporated matter is
included in accordance with the requirements of regulation 5 of the Subordinate
Legislation Regulations 2004.
Statutory Rule
Provision
Title of applied, adopted or
incorporated document
Matter in
applied,
adopted or
incorporated
document
Regulation 4
(definition of "listed
regulated poison")
Poisons Code Part 2 of
Chapter 1
Regulation 4
(definition of
"ovulatory
stimulant")
Poisons Code Part 2 of
Chapter 1
Regulation 4
(definition of
"prostaglandin")
Poisons Code Part 2 of
Chapter 1
Endnotes
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Statutory Rule
Provision
Title of applied, adopted or
incorporated document
Matter in
applied,
adopted or
incorporated
document
Regulation 4
(definition of
"retinoid")
Poisons Code Part 2 of
Chapter 1
Regulation 4
(definition of "special
Schedule 7
substance")
Poisons Code which
incorporates:
Appendix C of Part 5 of the
Standard for the Uniform
Scheduling of Drugs and
Poisons as in force from time
to time
Part 2 of
Chapter 1
Endnotes
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INDEX
Subject Regulation
Act (def.) 4
Aged care services
approved providers (def.) 4
definition 4
high level of residential care (def.) 4
providers' duties regarding Schedule 4, 8, 9 poisons 36, 39–44, 70
See also Licences, permits and warrants
Ambulance services operational staff 5, 36, 39, 46, 70
Amphetamines 22, Sch. 2
Animals 12–13
See also Prescriptions; Veterinary practitioners
Attention deficit disorder 22
Authorised optometrists
dealings in Schedule 4 poisons
emergency supply on oral instructions of 27, 47
labelling 29
notice of loss, theft 70
notice of poisons obtained fraudulently 14
orders for administration of 46
storage 34
therapeutic need for 11
definition 4
See also Prescriptions; Records
Carriers 5
Definitions 4, 38
Dental auxiliaries 5, 36, 39, 46, 70
Dentists
dealings in drugs of dependence 10
dealings in Schedule 3 poisons 60, 63
dealings in Schedule 4, 8, 9 poisons
emergency supply on oral instructions of 27, 47
labelling 29
orders for administration of 46
patient identity and therapeutic need for 10
permits required for Schedule 9 poisons 7
storage 34–35
drugs, poisons dentists prohibited from dealing in 23, 55
notice of drugs, poisons obtained fraudulently 14
notice of loss, theft of poisons, substances 70
See also Prescriptions; Records
Dexamphetamine 22, Sch. 2
Drug-dependent persons 18–20, Sch. 2
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Subject Regulation
Drugs of dependence
disclosure of use within previous 8 weeks 24
for animals 12–13
obtained fraudulently 14
patient identity, therapeutic need 8, 10, 12–13
permits for specialised supply, treatment with 19–22, Sch. 2
prohibited supply, administration 49, 64
storage 35
See also Prescriptions
Schedule 8 and Schedule 9 poisons
Environmental health officers 5, 36, 39, 46, 70
Etorphine permit holders
See Licences, permits and warrants
Labelling and packaging 29, 68–69
Licences, permits and warrants
agents of holders of 5
etorphine permit holders 5, 36, 39, 46, 70
fees 75
holders of
notice of loss, theft of poisons, substances by 70
possession, use of Schedule 4, 8, 9 poisons by 5
records kept by 39–44
restriction of access to poisons, substances by 71
storage, display of Schedule 3 poisons by 62
storage of Schedule 4, 8, 9 poisons by 34–35
licences to sell, supply Schedule 2 poisons by retail 74
permits for Schedule 9 poisons 7
permits for specialised supply of Schedule 8, 9
poisons 19–22, Sch. 2
required for listed regulated poisons 65
required for special Schedule 7 substances 67
warrants for ovulatory stimulants, prostaglandins,
retinoids, thalidomide 53–54
Listed regulated poisons See Schedule 7 poisons
Medical practitioners
dealings in ovulatory stimulants, prostaglandins,
retinoids, thalidomide 53–54
dealings in Schedule 3 poisons 57, 63
dealings in Schedule 4, 8, 9 poisons, drugs of
dependence
emergency supply on oral instructions of 27, 47
labelling 29
orders for administration of 46
patient identity and therapeutic need for 8
permits for Schedule 9 poisons 7
permits for specialised supply, treatment with 19–22, Sch. 2
storage 34–35
notice of drug-dependent persons 18, Sch. 2
notice of drugs, poisons obtained fraudulently 14
notice of loss, theft of poisons, substances 70
See also Prescriptions; Records
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Subject Regulation
Methadone 19, 21, 23, Sch. 2
Methylamphetamine 22, Sch. 2
Methylphenidate 22, Sch. 2
Narcotic plants 52
Nurse practitioners
dealings in Schedule 3 poisons 58, 63
dealings in Schedule 4, 8 poisons
emergency supply on oral instructions of 27, 47
labelling 29
notice of poisons obtained fraudulently 14
orders for administration of 46
patient identity and therapeutic need for 9
permits for specialised supply, treatment with 19–22, Sch. 2
storage 34–35
notice of drug-dependent persons 18, Sch. 2
notice of loss, theft of poisons, substances 70
prescribed poisons according to categories of 56, Sch. 3
See also Prescriptions; Records
Nurses
authorised to possess Schedule 4, 8, 9 poisons 5
administration of drugs, poisons by 46–47
definition 4
notice of loss, theft of poisons, substances 70
records kept by 39–44
storage of Schedule 4, 8, 9 poisons 34–36
Optometrists 5, 36, 39, 46, 70
See also Authorised optometrists
Orthoptists 4, 5, 36, 39, 46, 70
Ovulatory stimulants 4, 53–55
Packaging See Labelling and packaging
Palliative care services 4, 21
Permits See Licences, Permits and warrants
Pharmacists
dealings in drugs of dependence 12
dealings in Schedule 3 poisons 61, 63
dealings in Schedule 4, 8, 9 poisons
emergency supply by 15, 27
labelling 29
permits required for Schedule 9 poisons 7
sales, supply of Schedule 4, 8 poisons 15–17
storage 34–35
notice of drugs, poisons obtained fraudulently 14
notice of loss, theft of poisons, substances 70
notice of similar supply by different prescribers 32
See also Prescriptions; Records
Podiatrists 4, 5, 36, 39, 46, 70
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Subject Regulation
Prescriptions
circumstances where not to be filled 31
details included in records of transactions 40
duration 30
for animals 25–26
fraudulent, forged prescriptions 14, 31
from different prescribers for similar supply 32
information included in 26
interstate prescriptions 17
marking upon supply 30, 33
oral instructions confirmed by 27
persons authorised to write 25
required for sale, supply by pharmacists 15
requirements in general 25–26
restrictions on dentists 26
retention, production on demand 33
supply on copies of 16
verification of certain details before supply 28
Prostaglandins 4, 53–55
Records
definition of transactions for which required 38
details contained in 40
false, misleading entries 42
investigation of discrepancies 43
loss, destruction, theft 44
of destruction of Schedule 8, 9 poisons 40, 51
persons required to keep 39
retention, retrieval, production on demand 41
Registered dental auxiliaries See Dental auxiliaries
Regulations
authorising provisions 2
objectives 1
revocations 3, Sch. 1
transitional provisions 76
Retinoids 4, 53–55
Revocations 3, Sch. 1
Sales (General) 68
Schedule 2 poisons 56, 74–75, Sch. 3
Schedule 3 poisons
prescribed according to nurse practitioner category 56, Sch. 3
prohibited supply, administration 64
requirements of supply, storage and display 62–63
therapeutic need for 57–61
See also Licences, permits and warrants
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Subject Regulation
Schedule 4 poisons
approval for possession, use 6
emergency supply 15, 27
for animals 13
labelling 29
obtained fraudulently 14
patient identity, therapeutic need for 8–11, 13
persons authorised to possess, use 5
prescribed according to nurse practitioner category 56, Sch. 3
restriction of access to 71
sales, supply by pharmacists 15–17
storage 34, 36–37
use, administration in general 45–49
See also Licences, permits and warrants;
Prescriptions; Records
Schedule 7 poisons
listed regulated poisons 4, 65, 71
notice of loss, theft by sellers, suppliers of 70
special Schedule 7 substances 4, 67
storage requirements 66
See also Licences, permits and warrants
Schedule 8 and Schedule 9 poisons
destruction 40, 50–51
emergency supply 15, 27
labelling 29
notice of treatment with 19, Sch. 2
obtained fraudulently 14
permits for specialised supply, treatment with 19–22, Sch. 2
permits required for Schedule 9 poisons 7
persons authorised to possess, use 5
restriction of access to 71
Schedule 8 poisons
approval for possession, use 6
for animals 13
patient identity, therapeutic need for 8–10, 13
prescribed for nurse practitioner category 56, Sch. 3
sales, supply by pharmacists 15–16
storage 35–37
use, administration in general 45–49
See also Licences, permits and warrants;
Prescriptions; Records
Secretary
functions, powers regarding
approval of Schedule 4, 8 poisons 6
authority to cultivate narcotics 52
destruction of Schedule 8, 9 poisons 51
licences, permits 20–22, 74
nurses 5
prescriptions 26
storage 37
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Subject Regulation
Seizure 72–73, Sch. 2
Ship masters, officers, crew members 5, 36, 39, 46, 70
Ski patrollers 5, 36, 39, 46, 70
Special Schedule 7 substances See Schedule 7 poisons
St John Ambulance members 5, 36, 39, 46, 70
State Emergency Services
dealings in Schedule 4, 8 poisons by directors of 5, 36, 39, 46, 70
Storage 4, 34–37, 66
Thalidomide 53–55
Transitional provisions 76
Veterinary practitioners
dealings in drugs of dependence 13
dealings in Schedule 3 poisons 59, 63
dealings in Schedule 4, 8, 9 poisons
emergency supply on oral instructions of 27
labelling 29
permit for Schedule 9 poisons 7
storage 34–35
therapeutic need for 13
notice of drugs, poisons obtained fraudulently 14
notice of loss, theft of poisons, substances 70
See also Prescriptions; Records
Warrants See Licences, permits and warrants
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