Drugs, Poisons and Controlled Substances Amendment (Real-time Prescription Monitoring) Act 2017
Authorised by the Chief Parliamentary Counsel
Authorised Version
i
Drugs, Poisons and Controlled Substances
Amendment (Real-time Prescription Monitoring)
Act 2017
No. 50 of 2017
TABLE OF PROVISIONS
Section Page
1 Purpose 1
2 Commencement 2
3 Principal Act 2
4 Definitions 2
5 New Division 9 of Part II inserted 4
6 Definitions 12
7 New section 32A inserted 13
8 Repeal of Subdivision 2 of Division 10 of Part II 14
9 Section 34D substituted 14
10 Exception to Schedule 8 permit requirement—patients in
prisons, aged care services and hospitals 15
11 Section 35A substituted 15
12 Section 36 repealed 15
13 Inspections 16
14 New section 42A inserted 16
15 Evidentiary 16
16 Regulations 17
17 General regulations 17
18 New section 146 inserted 18
19 Repeal of amending Act 19
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Endnotes 20
1 General information 20
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Authorised by the Chief Parliamentary Counsel
Authorised Version
1
Drugs, Poisons and Controlled
Substances Amendment (Real-time
Prescription Monitoring) Act 2017 †
No. 50 of 2017
[Assented to 24 October 2017]
The Parliament of Victoria enacts:
1 Purpose
The main purpose of this Act is to amend the
Drugs, Poisons and Controlled Substances
Act 1981 to provide for—
(a) a database relating to the monitoring of the
supply of certain poisons and controlled
substances; and
Victoria
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(b) information to be included on the database;
and
(c) access to the database.
2 Commencement
(1) Subject to subsection (2), this Act comes into
operation on a day or days to be proclaimed.
(2) If a provision of this Act does not come into
operation before 1 August 2018, it comes into
operation on that day.
3 Principal Act
In this Act, the Drugs, Poisons and Controlled
Substances Act 1981 is called the Principal Act.
4 Definitions
In section 4(1) of the Principal Act insert the
following definitions—
"authorised supplier means a person who—
(a) is authorised by the Secretary under
section 30C(5) to access the monitored
poisons database for a purpose
specified in section 30C(5)(a); or
(b) is authorised by regulations referred
to in section 30C(4) to access the
monitored poisons database; or
(c) belongs to a class of person that is
authorised as described in paragraph (a)
or (b);
authorised user means a person who—
(a) is authorised by the Secretary under
section 30C(5) to access the monitored
poisons database for a purpose
specified in section 30C(5)(b) or (c); or
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(b) is authorised by regulations referred
to in section 30C(4) to access the
monitored poisons database; or
(c) belongs to a class of person that is
authorised as described in paragraph (a)
or (b);
data source entity means an entity, or a class of
entity, prescribed to be a data source entity
for the purposes of the monitored poisons
database;
monitored poison means—
(a) a Schedule 8 poison; or
(b) a monitored supply poison; or
(c) a poison that is prescribed to be a
monitored poison; or
(d) a poison that belongs to a class of
poisons that are prescribed to be
monitored poisons;
monitored poisons database means the database
established under Division 9 of Part II;
monitored supply poison means a poison that—
(a) is prescribed to be a monitored supply
poison; or
(b) belongs to a class of poisons that are
prescribed to be monitored supply
poisons;
registered health practitioner means a person
registered under the Health Practitioner
Regulation National Law to practise in a
health profession within the meaning of
that Law (other than as a student);".
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5 New Division 9 of Part II inserted
After Division 8 of Part II of the Principal Act
insert—
"Division 9—Monitored poisons
database
30A Secretary may establish monitored
poisons database
(1) The Secretary may establish and maintain a
database for the purposes of monitoring and
recording data relating to the supply of
monitored poisons.
(2) The monitored poisons database may include
the following—
(a) a record for each supply of a monitored
poison in accordance with the
regulations;
(b) a record of applications for permits
made to the Secretary, notifications
provided to the Secretary and
permits issued by the Secretary
under Division 10, this Division or
the regulations in relation to the
supply to, or treatment of, persons
with poisons or controlled substances;
(c) a record of applications for warrants
made to the Secretary, and warrants
issued by the Secretary, under
Division 4 of Part II in relation to the
supply to, or treatment of, persons with
poisons or controlled substances;
(d) any other prescribed information.
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30B Powers of Secretary in relation to
monitored poisons database
(1) The purposes of the monitored poisons
database are—
(a) to promote safe supply, prescription
and dispensing practices; and
(b) to reduce harm from monitored poisons
and other high risk medication; and
(c) to facilitate evaluation and research into
monitored poisons and the operation of
the monitored poisons database.
(2) For the purposes of establishing and
maintaining the monitored poisons database
and furthering the purposes of the database,
the Secretary may—
(a) collect and store information
(including records) required for the
database or permitted to be collected
and stored by or under this Act or the
regulations; and
(b) require a prescribed person or
prescribed class of person or a data
source entity to provide information
(including records) to the database in
accordance with the regulations; and
(c) require prescribed records or prescribed
information in relation to the supply of
a monitored poison to be provided to
the monitored poisons database in the
prescribed manner or in the prescribed
form; and
(d) use and disclose any information on
the database reasonably necessary to
implement and oversee the database,
including but not limited to—
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(i) disclosing information on the
database to the Commonwealth,
other States or Territories; and
(ii) receiving or collecting
information for the database from
the Commonwealth, other States
or Territories or prescribed entities
in other Australian jurisdictions;
and
(iii) authorising in writing other
prescribed entities to use and
disclose information on the
database; and
(iv) use and disclosure of information
on the database in accordance
with this Act or the regulations;
and
(e) do any other thing or exercise any other
power reasonably necessary—
(i) to implement, maintain and
oversee the database; or
(ii) further the purposes of the
database.
(3) Without limiting subsection (2) or any other
power of the Secretary, the Secretary may
enter into an agreement or a memorandum
of understanding with the Commonwealth,
other States or Territories and any entity in
another Australian jurisdiction in relation to
the provision of information to or from the
monitored poisons database by or to that
other jurisdiction.
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30C Access, use and disclosure of information
on monitored poisons database
(1) A pharmacist may access, use and disclose
information on the monitored poisons
database for the following specified
purposes—
(a) providing records and information to
the database in accordance with this
Act or the regulations;
(b) accessing records and information
in relation to a person for whom a
monitored poison may be supplied;
(c) accessing records and information in
relation to a person in relation to the
medical treatment or care of that
person;
(d) disclosing information in the database
to any registered health practitioner
involved in the care of a person whose
information is maintained in the
database;
(e) any other prescribed purpose.
(2) A registered medical practitioner or a nurse
practitioner may access, use and disclose
information on the monitored poisons
database for the following specified
purposes—
(a) providing records and information to
the database in accordance with this
Act or the regulations;
(b) accessing records and information
in relation to a person for whom a
monitored poison may be supplied,
prescribed or administered;
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(c) accessing records and information in
relation to a person in relation to the
medical treatment or care of that
person;
(d) disclosing information in the database
to any registered health practitioner
involved in the care of a person whose
information is maintained in the
database;
(e) any other prescribed purpose.
(3) Any person who is authorised by the
Secretary under subsection (5), or who
belongs to a class of person that is authorised
by the Secretary under subsection (5), may
access, use and disclose information on the
monitored poisons database for the purposes
specified in that authorisation.
(4) Any entity that is prescribed, or that belongs
to a prescribed class, may access, use and
disclose information on the monitored
poisons database for the purposes specified
in relation to the entity in the regulations.
(5) The Secretary may authorise a person or
class of person to access, use and disclose
information in the monitored poisons
database for the purposes specified in
relation to the person or class in the
authorisation if satisfied that the access,
use and disclosure—
(a) would assist in achieving the purposes
of—
(i) promoting safe supply,
prescription and dispensing
practices; and
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(ii) reducing harm from monitored
poisons and other high risk
medication; or
(b) is for technical or administrative
purposes relating to the maintenance of
the database; or
(c) is to facilitate evaluation and research
into monitored poisons and the
operation of the monitored poisons
database.
(6) An authorisation under subsection (5)
must—
(a) be in writing; and
(b) in the case of an authorisation for a
class of person, be published in the
Government Gazette.
Note
See also section 42A in relation to authorized officers.
30D Data source entity to provide records and
information to monitored poisons
database
Unless the regulations otherwise provide,
a data source entity must take all reasonable
steps to ensure that all records or information
in relation to the supply of a monitored
poison are provided to the monitored poisons
database in the manner or in the form
prescribed for the purposes of section
30B(2).
Penalty: 100 penalty units.
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30E Pharmacist to check monitored poisons
database before supply of monitored
supply poison
Unless the regulations otherwise provide, a
pharmacist must take all reasonable steps to
check the monitored poisons database for the
records or information in relation to a person
for whom a monitored supply poison may be
supplied before supplying the monitored
supply poison for that person.
Penalty: 100 penalty units.
30F Registered medical practitioner to check
monitored poisons database before
prescription or supply of monitored
supply poison
Unless the regulations otherwise provide, a
registered medical practitioner must take all
reasonable steps to check the monitored
poisons database for the records or
information in relation to a person for
whom a monitored supply poison may be
prescribed or supplied before prescribing or
supplying the monitored supply poison for
that person.
Penalty: 100 penalty units.
30G Nurse practitioner to check monitored
poisons database before prescription or
supply of monitored supply poison
Unless the regulations otherwise provide, a
nurse practitioner must take all reasonable
steps to check the monitored poisons
database for the records or information in
relation to a person for whom a monitored
supply poison may be prescribed or supplied
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before prescribing or supplying the
monitored supply poison for that person.
Penalty: 100 penalty units.
30H Authorised supplier to check monitored
poisons database before prescription or
supply of monitored supply poison
Unless the regulations otherwise provide, an
authorised supplier must take all reasonable
steps to check the monitored poisons
database for the records or information in
relation to a person for whom a monitored
supply poison may be prescribed or supplied
by that authorised supplier in accordance
with the supplier's authorisation before
prescribing or supplying the monitored
supply poison for that person.
Penalty: 100 penalty units.
30I Offences relating to access or use of
monitored poisons database unless
authorised
(1) A person who is not authorised to do so
by or under this Act, the regulations or
otherwise by any law must not knowingly
access, use or disclose information on the
monitored poisons database.
Penalty: 100 penalty units.
(2) A person who is authorised to do so by or
under this Act, the regulations or otherwise
by any law to access, use or disclose
information on the monitored poisons
database must not access, use or disclose
information on the monitored poisons
database other than in accordance with the
person's authorisation.
Penalty: 100 penalty units.
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30J Protection from liability for duties and
functions in relation to monitored poisons
database
(1) A registered medical practitioner, nurse
practitioner, pharmacist, authorised supplier
or authorised user is not liable for anything
done in good faith in carrying out any duty
or function in relation to the monitored
poisons database in accordance with this
Act or the regulations.
(2) Without limiting subsection (1)—
(a) the accessing of information on the
monitored poisons database in respect
of a person or the providing of
information to the database in respect
of a person does not constitute
unprofessional conduct or a breach of
professional etiquette or ethics; and
(b) no liability for defamation is incurred
by a person referred to in subsection (1)
because of the accessing of any person's
information or the provision of that
information.".
6 Definitions
(1) In section 31(1) of the Principal Act, for the
definition of hospital substitute—
"hospital means the following—
(a) a public hospital within the meaning of
the Health Services Act 1988;
(b) a denominational hospital within the
meaning of that Act;
(c) a private hospital within the meaning of
that Act;
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(d) a day procedure centre within the
meaning of that Act;".
(2) In section 31(1) of the Principal Act—
(a) insert the following definition—
"reportable drug event has the meaning
given in section 32A(2);";
(b) the definition of notification of
drug-dependent person is repealed.
7 New section 32A inserted
After section 32 of the Principal Act insert—
"32A Required notification to Secretary—drugs
of dependence and Schedule 4, Schedule 8
and Schedule 9 poisons
(1) A registered medical practitioner, a nurse
practitioner or a pharmacist must notify
the Secretary as soon as practicable of a
reportable drug event.
Penalty: 100 penalty units.
(2) For the purposes of subsection (1), a
reportable drug event is one or more of the
following—
(a) for a pharmacist, being requested or
directed to sell, supply or dispense any
drug of dependence, Schedule 8 poison,
Schedule 9 poison or Schedule 4 poison
for any person—
(i) in greater quantities than appears
to be reasonably necessary; or
(ii) more frequently than appears to be
reasonably necessary;
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(b) for a registered medical
practitioner, having reason to
believe that the practitioner's
patient is a drug-dependent person
in circumstances where—
(i) the patient requests or seeks
prescription of a Schedule 9
poison; or
(ii) the registered medical practitioner
intends to treat or is treating the
patient with a Schedule 9 poison;
(c) any other event, or class of event,
which the Secretary declares, under
subsection (3), is a reportable drug
event.
(3) For the purposes of this section, the
Secretary, by notice published in the
Government Gazette, may declare an event,
or a class of event (including any event that
occurs outside Victoria), to be a reportable
drug event.".
8 Repeal of Subdivision 2 of Division 10 of Part II
Subdivision 2 of Division 10 of Part II of the
Principal Act is repealed.
9 Section 34D substituted
For section 34D of the Principal Act substitute—
"34D Exception to Schedule 8 permit
requirement—specified circumstances
Despite section 34C(1), a registered
medical practitioner or a nurse practitioner is
authorised to administer, supply or prescribe
a Schedule 8 poison to or for a person who is
not a drug-dependent person during a
continuous period greater than 8 weeks
without a Schedule 8 permit if the
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administration, supply or prescription of that
Schedule 8 poison is to treat that person in
the circumstances specified by the Secretary
in accordance with section 35A.".
10 Exception to Schedule 8 permit requirement—
patients in prisons, aged care services and hospitals
In section 34F(c) of the Principal Act, after
"hospital" insert "or a patient being treated in an
emergency department of a hospital, for the period
of that treatment in the hospital and a period not
exceeding 7 days after that person's discharge
from the hospital".
11 Section 35A substituted
For section 35A of the Principal Act substitute—
"35A Secretary may specify circumstances for
purposes of section 34D
(1) The Secretary, by notice published in
the Government Gazette, may specify
circumstances in which a registered
medical practitioner or a nurse practitioner is
authorised to administer, supply or prescribe
a Schedule 8 poison to or for a person who
is not a drug-dependent person during a
continuous period greater than 8 weeks
without a Schedule 8 permit for the purposes
of section 34D.
(2) The Secretary, by notice published in the
Government Gazette, may amend or revoke
a notice under subsection (1).".
12 Section 36 repealed
Section 36 of the Principal Act is repealed.
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13 Inspections
After section 42(1)(b) of the Principal Act
insert—
"(ba) access and examine or inspect records or
information required to be included on the
monitored poisons database;".
14 New section 42A inserted
After section 42 of the Principal Act insert—
"42A Powers of authorized officers to access,
use and disclose information on monitored
poisons database
Without limiting section 42, an authorized
officer may access the monitored poisons
database and use and disclose information
on that database for the purposes of—
(a) implementing and monitoring the use
of the database and the records and
information in the database; and
(b) carrying out any other function or
power as an authorized officer under
this Act and the regulations.".
15 Evidentiary
(1) In section 119(f) of the Principal Act, for "stated."
substitute "stated;".
(2) After section 119(f) of the Principal Act insert—
"(g) a certificate signed by the Secretary that a
document is an extract from the monitored
poisons database is prima facie evidence of
the facts stated in that extract.".
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16 Regulations
After section 129(1)(ca) of the Principal Act
insert—
"(cb) prescribing, for the purposes of Division 9 of
Part II, any matter necessary or required in
relation to—
(i) the monitored poisons database; or
(ii) providing, accessing, using or
disclosing information on the
monitored poisons database to, or
receiving and using information
from, entities or health practitioners
in Victoria or other States, the
Territories or the Commonwealth; or
(iii) prescribing locations, geographical
areas or regions in which Division 9,
or specified provisions of that Division,
are to operate, or not to operate, for any
specified period of time or subject to
specified conditions; or
(iv) any other matter under that Division;".
17 General regulations
After section 132(zce) of the Principal Act
insert—
"(zcf) without limiting section 129, prescribing,
for the purposes of Division 9 of Part II, any
matter necessary or required in relation to—
(i) the monitored poisons database; or
(ii) providing, accessing, using or
disclosing information on the
monitored poisons database to, or
receiving and using information from,
entities or health practitioners in
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Victoria or other States, the Territories
or the Commonwealth; or
(iii) any other matter under that Division;".
18 New section 146 inserted
At the end of Part XII of the Principal Act
insert—
"146 Transitional provisions—Drugs, Poisons
and Controlled Substances Amendment
(Real-time Prescription Monitoring)
Act 2017—staged implementation area
(1) Despite the commencement of Division 9 of
Part II, sections 30E, 30F, 30G and 30H do
not apply in any staged implementation area
for a period not exceeding 12 months after
the commencement of that Division.
(2) Subject to subsection (3), the Minister, by
order published in the Government Gazette,
may—
(a) declare an area or more than one area to
be a staged implementation area; and
(b) specify the period, not exceeding
12 months, during which the area is a
staged implementation area.
(3) The Minister must not make an order under
subsection (2) unless satisfied that—
(a) the monitored poisons database has not
been made accessible by the Secretary
in the area to which the order is to
apply; and
(b) it is appropriate to disapply those
sections for the period specified in the
order.
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(4) In this section staged implementation area
means any location or area specified by the
Minister in an order under subsection (2).
(5) This section is repealed on the second
anniversary of its commencement.".
19 Repeal of amending Act
This Act is repealed on 1 July 2019.
Note
The repeal of this Act does not affect the continuing
operation of the amendments made by it (see section 15(1)
of the Interpretation of Legislation Act 1984).
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Endnotes
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Endnotes
1 General information
See www.legislation.vic.gov.au for Victorian Bills, Acts and current
authorised versions of legislation and up-to-date legislative information.
† Minister's second reading speech—
Legislative Assembly: 9 August 2017
Legislative Council: 7 September 2017
The long title for the Bill for this Act was "A Bill for an Act to amend the
Drugs, Poisons and Controlled Substances Act 1981 to provide for a
database relating to the monitoring of the supply of certain poisons and
controlled substances, to provide for use of the database and for other
purposes."
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