Rail Safety (Local Operations) (Drug and Alcohol Controls) Regulations 2017
Authorised by the Chief Parliamentary Counsel
Authorised Version
i
Rail Safety (Local Operations) (Drug and Alcohol
Controls) Regulations 2017
S.R. No. 78/2017
TABLE OF PROVISIONS
Regulation Page
Part 1—Preliminary 1
1 Objective 1
2 Authorising provision 1
3 Commencement 1
4 Definitions 2
Part 2—Drug and alcohol controls 3
5 Preliminary breath test devices 3
6 Procedure for breath analysis 3
7 Procedure for taking blood sample 3
8 Procedure after taking blood samples 4
9 Certificate under section 85(8) 5
10 Particulars of report of assessment of drug impairment 6
11 Certificate under section 86I(5) 8
12 Certificate under section 86I(6) 8
13 Certificate under section 86I(7) 9
14 Certificate under section 86I(8) 10
15 Devices prescribed for the purposes of oral fluid analysis and
drug screening tests 10
16 Procedure for carrying out oral fluid analysis or drug screening
tests 11
17 Procedure after taking oral fluid sample 11
18 Certificate under section 86J(5) 12
19 Certificate under section 86J(6) 12
20 Certificate under section 86J(7) 13
21 Duty to provide indicative positive results to Safety Director 13
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Endnotes 15
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Authorised by the Chief Parliamentary Counsel
Authorised Version
1
STATUTORY RULES 2017
S.R. No. 78/2017
Rail Safety (Local Operations) Act 2006
Rail Safety (Local Operations) (Drug and Alcohol
Controls) Regulations 2017
The Governor in Council makes the following Regulations:
Dated: 18 July 2017
Responsible Minister:
JACINTA ALLAN
Minister for Public Transport
ANDREW ROBINSON
Clerk of the Executive Council
Part 1—Preliminary
1 Objective
The objective of these Regulations is to promote
safe rail operations in Victoria by prescribing
requirements for drug and alcohol controls for rail
safety workers.
2 Authorising provision
These Regulations are made under section 109 of
the Rail Safety (Local Operations) Act 2006.
3 Commencement
These Regulations come into operation on 21 July
2017.
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4 Definitions
In these Regulations, the Act means the Rail
Safety (Local Operations) Act 2006.
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Part 2—Drug and alcohol controls
5 Preliminary breath test devices
The devices prescribed for the purposes of
section 84 of the Act are the breath testing
devices known as—
(a) the lion alcolmeter SD-400 Touch; and
(b) the Lion Alcolmeter also known as the
lion alcolmeter S-D2; and
(c) the lion alcolmeter SD-400PA; and
(d) the Alcolizer LE; and
(e) AlcoQuant 6020.
6 Procedure for breath analysis
It is a requirement for the proper operation
of a breath analysing instrument that a person
authorised under section 85(7) of the Act to
operate a breath analysing instrument—
(a) does not require a person to provide a breath
sample for analysis until the authorised
person is satisfied that the person has not
consumed any alcohol for a period of at
least 15 minutes before the analysis; and
(b) provides a fresh mouthpiece for use by each
person required to provide a breath sample;
and
(c) uses only a mouthpiece which, until required
for taking the breath sample, has been kept in
a sealed container.
7 Procedure for taking blood sample
If a blood sample is taken by a registered medical
practitioner or an approved health professional for
the purposes of the Act, the site of the puncture
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must be cleansed with a swab taken from a
container which—
(a) appears to be sealed against contamination;
and
(b) bears a label stating that the container holds
an aqueous solution of chlorohexidine and
cetrimide and no methylated spirits, alcohol,
tincture of iodine or other substance
containing alcohol.
8 Procedure after taking blood samples
(1) A registered medical practitioner or an approved
health professional who takes a blood sample
must ensure that—
(a) the sample of blood is placed in 3 dry
containers, each containing approximately
the same amount of blood; and
(b) each container is vacuum sealed or sealed
with a septum seal; and
(c) each container in which the sample is placed
bears a label stating—
(i) that the container holds a specific
anti-coagulant and preservative such as
potassium oxalate and sodium fluoride;
and
(ii) the name of the chemist, laboratory
or pharmaceutical organisation that
prepared the container; and
(d) each container has attached to it a label
bearing the signature of the registered
medical practitioner or approved health
professional, the date and the time the
blood sample was taken, and the name of
the person from whom the sample was
taken or, if the name of the person is not
known, sufficient information to enable
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the sample to be identified with the person
from whom it was taken.
(2) If a blood sample is taken under section 85 of
the Act, the registered medical practitioner or
approved health professional must give one of
the containers to a police officer and another to
the person from whom the sample was taken.
(3) If a blood sample is taken under section 86H
of the Act and has, in accordance with this
regulation, been placed in containers which have
been sealed and labelled, the registered medical
practitioner or approved health professional must
ensure that—
(a) one container is placed in a locked receptacle
provided for the purpose at the place at
which the sample was taken; and
(b) one container is placed and sealed in a
container labelled "screening sample"; and
(c) one container is delivered to the person
from whom the blood sample was taken or
placed with that person's personal property
at the place at which the sample was taken.
9 Certificate under section 85(8)
A certificate given under section 85(8) of the Act
must contain the following particulars—
(a) the serial number of the breath analysing
instrument;
(b) the sample number;
(c) the location of the test;
(d) the name and date of birth of the person
whose breath is analysed;
(e) the surname of the operator;
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(f) the results of the self tests conducted by
the breath analysing instrument before and
after the person's breath is analysed;
(g) the results of zero tests conducted by the
breath analysing instrument before and
after the person's breath is analysed;
(h) the date and time the person's breath was
analysed.
10 Particulars of report of assessment of drug
impairment
For the purposes of section 86D(7) of the Act,
a report of assessment of drug impairment must
contain the following particulars—
(a) particulars of the identity of the person
on whom the assessment was carried out,
including, if known, the person's name,
address, date of birth and gender;
(b) the date and time at which the person
underwent the assessment;
(c) the place at which the person underwent
the assessment;
(d) the time (if any) reported to the transport
safety officer or police officer (as the case
requires) carrying out the assessment as the
latest time the person carried out rail safety
work;
(e) whether the person underwent a preliminary
breath test in accordance with section 83 of
the Act or furnished a sample of breath for
analysis by a breath analysing instrument
and, if so, the result of the test or analysis, if
known;
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(f) the record of interview of the person carried
out by the transport safety officer or the
police officer carrying out the assessment;
(g) particulars of any medical treatment sought
by or for the person;
(h) any statements made by the person
concerning a drug or drugs;
(i) any observations made by the transport
safety officer or police officer carrying out
the assessment of the person in relation to—
(i) any apparent injury or illness of the
person; and
(ii) whether the person smelt of
intoxicating liquor; and
(iii) the person's speech; and
(iv) the person's eyes; and
(v) the person's breathing; and
(vi) the person's skin; and
(vii) the person's movement; and
(viii) the person's balance; and
(ix) the state of the person's clothing; and
(x) the person's actions; and
(xi) the person's demeanour; and
(xii) any physical signs of drug use by the
person; and
(xiii) the person's ability to comprehend
instructions; and
(xiv) the person's ability to divide attention;
and
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(xv) whether the person, during the
assessment, exhibited signs that
indicated that the person was
impaired by a drug or drugs;
(j) whether the assessment, in the opinion of
the transport safety officer or police officer
carrying it out, indicates that the person may
be impaired by a drug or drugs;
(k) the name, identification number and
signature of the transport safety officer,
or the name, rank, station and signature
of the police officer (as the case requires)
carrying out the assessment.
11 Certificate under section 86I(5)
A certificate for the purposes of section 86I(5) of
the Act must contain the following particulars—
(a) a statement by the registered medical
practitioner or approved health professional
that the requirements of these Regulations
for the taking of blood samples have been
complied with;
(b) the name of the person from whom the blood
sample was taken;
(c) the time and date the blood sample was
taken;
(d) the name and signature of the registered
medical practitioner or approved health
professional who took the blood sample.
12 Certificate under section 86I(6)
A certificate for the purposes of section 86I(6)
of the Act must contain, in addition to a statement
as to the concentration of alcohol found in the
sample of blood, the following particulars—
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(a) a statement by the approved analyst that the
analyst is an approved analyst within the
meaning of section 86I(1) of the Act;
(b) a statement as to the method of analysis
used;
(c) the name and signature of the approved
analyst;
(d) the date the analysis was conducted;
(e) a description of the contents of the
identification label referred to in
regulation 8(1)(d) attached to the
container in which the blood sample
is placed.
13 Certificate under section 86I(7)
A certificate under section 86I(7) of the Act must
contain the following particulars—
(a) a statement by the approved analyst that
the analyst is an approved analyst within
the meaning of section 86I(1) of the Act;
(b) a statement as to the method of analysis
used;
(c) a statement that a substance that is, or is
capable of being, a drug for the purposes of
the Act was present in the sample of blood
analysed;
(d) the name of the substance found to be
present in the sample of blood analysed;
(e) the name and signature of the approved
analyst;
(f) the date on which the analysis was
conducted;
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(g) a description of the identification label
referred to in regulation 8(1)(d) attached
to the container in which the blood sample
is placed.
14 Certificate under section 86I(8)
A certificate under section 86I(8) of the Act must
contain the following particulars—
(a) a statement by the approved expert that
the expert is an approved expert within
the meaning of section 86I(1) of the Act;
(b) a statement as to the usual effect of a
specified substance or substances on
behaviour when consumed or used
(including the effect on a person's ability
to carry out rail safety work properly);
(c) the name and signature of the approved
expert.
15 Devices prescribed for the purposes of oral fluid
analysis and drug screening tests
For the purposes of the definitions of drug
screening test and oral fluid analysis in
section 70 of the Act, the following devices
are prescribed—
(a) the oral fluid testing device known as the
SECURETEC DRUGWIPE TWIN or the
SECURETEC DRUGWIPE II TWIN;
(b) the oral fluid testing device known as the
SECURETEC DRUGWIPE II TWIN
COMBO;
(c) the oral fluid testing device known as the
Cozart RapiScan;
(d) the oral fluid screening device known as the
Medvet Oral7;
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(e) the oral fluid screening device known as the
Ultrasal-2 Saliva Collection Device;
(f) the oral fluid analysis device known as the
Thermo TSQ Quantum Ultra;
(g) the oral fluid analysis device known as the
Thermo TSQ Quantum Access;
(h) the oral fluid analysis device known as the
Thermo LTQ Orbitrap Discovery;
(i) the oral fluid analysis device known as the
Sciex QTrap 4500 or 5500.
16 Procedure for carrying out oral fluid analysis or
drug screening tests
For the purposes of a drug screening test or oral
fluid analysis under section 86A of the Act, a
transport safety officer or a police officer who
conducts the test or analysis must—
(a) provide a fresh oral fluid collection unit for
use by a person required to submit to the
drug screening test or oral fluid analysis; and
(b) use only an oral fluid collection unit that
has been kept in a sealed container until it
is given to that person; and
(c) test or analyse any oral fluid sample
produced by that person by using the
device, or the oral fluid testing unit that
is part of the device through which the
sample was provided.
17 Procedure after taking oral fluid sample
A transport safety officer or a police officer who
is provided a sample of oral fluid by a person
under a requirement under section 86A of the
Act must ensure that the sample or, if the sample
is broken into parts, each part of the sample has
attached to it a label bearing—
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(a) the name and signature of the police officer
to whom the oral fluid sample was provided;
and
(b) the date and time the sample was provided;
and
(c) the name of the person who provided the
sample or, if the name of the person is not
known, sufficient information to enable the
sample to be identified with the person who
provided the sample.
18 Certificate under section 86J(5)
A certificate for the purposes of section 86J(5) of
the Act must contain the following particulars—
(a) a statement by the registered medical
practitioner or approved health professional
that the requirements of these Regulations
for the taking of blood samples have been
complied with;
(b) the name of the person from whom the oral
fluid sample was taken;
(c) the time and date the oral fluid sample was
taken;
(d) the name and signature of the registered
medical practitioner or approved health
professional who took the oral fluid sample.
19 Certificate under section 86J(6)
A certificate under section 86J(6) of the Act must,
in addition to a statement as to the presence of a
drug in that sample of oral fluid, contain the
following particulars—
(a) a statement by the approved analyst that
the analyst is an approved analyst within
the meaning of section 86J(1) of the Act;
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(b) a statement as to the method of analysis
used;
(c) the name and signature of the approved
analyst;
(d) the date on which the analysis was
conducted;
(e) a description of the contents of the
identification label referred to in
regulation 17 that was attached to
the part of the oral fluid received for
analysis.
20 Certificate under section 86J(7)
A certificate under section 86J(7) of the Act
must contain the following particulars—
(a) a statement by the approved expert that
the analyst is an approved expert within
the meaning of section 86J(1) of the Act;
(b) a statement as to the usual effect of a
specified substance or substances on
behaviour when consumed or used
(including its effect on a person's ability
to carry out rail safety work properly);
(c) the name and signature of the approved
expert.
21 Duty to provide indicative positive results to Safety
Director
(1) A rail transport operator must, within 48 hours
after becoming aware, notify the Safety Director
if a rail safety worker carrying out rail safety
work for the rail transport operator has undergone
a preliminary breath test, drug screening test or
an assessment of drug impairment and the test
statement indicates or shows a positive result.
Penalty: 10 penalty units.
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(2) A notification under subregulation (1) must
contain a statement of action specifying the
response and proposed action to be taken by
the rail transport operator against the rail
safety worker as a consequence of the positive
test result.
(3) A notification under subregulation (1) must be
in writing and must be in an approved form.
(4) In this regulation, positive result means—
(a) if the rail safety worker has undergone a
preliminary breath test, the test indicates
that the rail safety worker's breath contains
alcohol; or
(b) if the rail safety worker has undergone a
drug screening test, the test shows that the
rail safety worker may have a prescribed
drug present in his or her oral fluid or blood;
or
(c) if the rail safety worker has undergone
an assessment of drug impairment, the
assessment indicates that the rail safety
worker may be impaired by a drug.
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Endnotes
Penalty Units
These Regulations provide for penalties by reference to penalty units within
the meaning of section 110 of the Sentencing Act 1991. The amount of the
penalty is to be calculated, in accordance with section 7 of the Monetary
Units Act 2004, by multiplying the number of penalty units applicable by the
value of a penalty unit.
The value of a penalty unit for the financial year commencing 1 July 2017 is
$158.57.
The amount of the calculated penalty may be rounded to the nearest dollar.
The value of a penalty 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
penalty unit for a financial year must be published in the Government Gazette
and a Victorian newspaper before 1 June in the preceding financial year.
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