Government Bill
119—3
As reported from the committee of the whole House
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Hon Dr David Clark
The Parliament of New Zealand enacts as follows:
This Act is the Misuse of Drugs Amendment Act 2019.
This Act comes into force on the day after the date on which it receives the Royal assent.
This Act amends the Misuse of Drugs Act 1975 (the principal Act).
(1)
In section 2(1), definition of Class C controlled drug, after “includes”, insert “any temporary class drug and”.
“includes”
“any temporary class drug and”
(2)
In section 2(1), definition of controlled drug, after “includes”, insert “any temporary class drug and”.
(3)
In section 2(1), insert in its appropriate alphabetical order:
temporary class drug means any substance, preparation, mixture, or article specified as a temporary class drug by an order made under section 4C
After section 4B, insert:
The Minister may, by an order published in the Gazette, specify any substance, preparation, mixture, or article as a temporary class drug.
The Minister must not make an order if the substance, preparation, mixture, or article is already a Class A controlled drug, a Class B controlled drug, a Class C controlled drug (except a controlled drug analogue), or a precursor substance.
The Minister must not make an order unless satisfied that the substance, preparation, mixture, or article that is to be specified in the order—
poses, or may pose, a risk of harm to individuals or to society; and
has not been classified under this Act, except as a controlled drug analogue.
(4)
An order may describe the substance, preparation, mixture, or article by either or both of the following:
its chemical name, or one of its chemical names:
a description of the substance, preparation, mixture, or article, in the form that the Minister considers appropriate for the purposes of the order.
(5)
An order must state the date on which the order comes into force, and that date must not be earlier than the day after the date of the publication of the order in the Gazette.
This section applies to every temporary class drug while it remains subject to a temporary class drug order.
The temporary class drug must be treated for all purposes as if the drug were a controlled drug that is specified or described in Part 1 of Schedule 3.
See section 7(5) for a prosecutorial discretion that applies to possession and use offences for all controlled drugs (including temporary class drugs).
A substance that has a structure substantially similar to the temporary class drug must not be treated as a controlled drug analogue just because of that similarity.
While a temporary class drug order is in place, the Minister must seek advice, as the Minister considers appropriate, under section 5 or 5AA (or both) about the temporary class drug and its appropriate classification (if any, including as a precursor substance) under this Act.
As soon as possible after the publication of a temporary class drug order in the Gazette, the Director-General of Health must ensure that, while the order remains in force, both the order and information about its effects are available—
on the Ministry of Health’s Internet site, in an electronic form that is publicly accessible; and
in any other way that the Director-General considers appropriate in the circumstances.
A temporary class drug order expires at the earliest of—
the close of the day that is 1 year after the date on which the order came into force; and
the date on which the substance, preparation, mixture, or article is—
classified as a Class A controlled drug; or
classified as a Class B controlled drug; or
classified as a Class C controlled drug; or
added to Schedule 4 as a precursor substance; and
its revocation by the Minister by order in the Gazette.
A temporary class drug order may be renewed by the Minister—
before the date of its expiry as calculated under subsection (1); and
on 1 occasion only; and
only for the purpose of allowing sufficient time for the Minister to obtain the advice that is to be sought under section 4E(1).
A temporary class drug order is a disallowable instrument but not a legislative instrument for the purposes of the Legislation Act 2012 and must be presented to the House of Representatives under section 41 of that Act.
After section 7(4), insert:
To avoid doubt, it is affirmed that there is a discretion to prosecute for an offence against subsection (1)(a), and a prosecution should not be brought unless it is required in the public interest.
(6)
When considering whether a prosecution is required in the public interest, in addition to any other relevant matters, consideration should be given to whether a health-centred or therapeutic approach would be more beneficial to the public interest.
In Schedule 1, clause 1, insert in their appropriate alphabetical order:
5F-ADB: Methyl (2S)-2-{[1-(5-fluoropentyl)-1H-indazole-3-carbonyl]amino}-3,3-dimethylbutanoate
AMB-FUBINACA: Methyl (2S)-2-({1-[(4-fluorophenyl)methyl]-1H-indazole-3-carbonyl}amino)-3-methylbutanoate
This section amends the Psychoactive Substances Act 2013.
After section 9(3)(b), insert:
a substance, preparation, mixture, or article specified by an order made under section 4C of the Misuse of Drugs Act 1975 as a temporary class drug:
7 March 2019
Introduction (Bill 119–1)
12 March 2019
First reading and referral to Health Committee
1 July 2019
Reported from Health Committee (Bill 119–2)
30 July 2019
Second reading
6 August 2019
Committee of the whole House (Bill 119–3)