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The Misuse of Drugs (Designation) (Amendment No.2) Order (Northern Ireland) 2018

S.R. 2018/174 · Made 11 October 2018

Original text. legislation.gov.uk does not revise statutory instruments, so later amendments are not shown here. Changes made to it are listed under each provision when known.

Dangerous Drugs

Made 11th October 2018

Coming into operation 1st November 2018

The Department of Healthf1 makes the following Order in exercise of the powers conferred by section 7(4) and (5) of the Misuse of Drugs Act 1971f2, as adapted by section 7(9) of that Act and now vested in itf3 and after consultation with the Advisory Council on the Misuse of Drugs in accordance with section 7(7) of that Act.

Annotations to the whole text

Footnotes

f1

The Department of Health, Social Services and Public Safety was renamed the Department of Health by section 1(5) of the Departments Act (Northern Ireland) 2016 (c. 5) (N.I.)

f2

1971 c.38, as amended by section 151 of, and Schedule 17 to, the Police Reform and Social Responsibility Act 2011 (c. 13)

f3

S.R.&O. (N.I.) 1973 No. 504, Article 5(a) and S.I. 1999/283 (N.I.), Article 3(6)

Contents

  1. 1Citation, commencement and interpretation
  2. 2Amendment of the Misuse of Drugs (Designation) Order (Northern Ireland) 2001
  3. Signature
  4. Explanatory note

1Citation, commencement and interpretation

(1)

This Order may be cited as the Misuse of Drugs (Designation) (Amendment No.2) Order (Northern Ireland) 2018 and shall come into operation on 1st November 2018.

(2)

The Interpretation Act (Northern Ireland) 1954f1 shall apply to this Order as it applies to an Act of the Northern Ireland Assembly.

2Amendment of the Misuse of Drugs (Designation) Order (Northern Ireland) 2001

(1)

Schedule 1 to the Misuse of Drugs (Designation) Order (Northern Ireland) 2001f1 (which specifies the controlled drugs to which section 7(4) of the Misuse of Drugs Act 1971 applies) is amended as follows.

(2)

In paragraph 1(a) of Part 1f2 —

(a)

after “Cannabinol” insert “(not being the product specified in paragraph 5 (1) or (2) of Part 2 of this Schedule)”;

(b)

after “Cannabinol derivatives not being dronabinol or its stereoisomers” insert “(and not being the product specified in paragraph 5(1) or (2) of Part 2 of this Schedule)”;

(c)

for “Cannabis (not being the substance specified in paragraph 4 of Part 2 of this Schedule)”, substitute “Cannabis (not being the substance specified in paragraph 4 of Part 2 of this Schedule or product specified in paragraph 5(1) or (2) of Part 2 of this Schedule)”; and

(d)

after “Cannabis resin” insert “(not being the product specified in paragraph 5(1) or (2) of Part 2 of this Schedule)”.

(3)

In Part 2 (which specifies controlled drugs excepted from Part 1), after paragraph 4 insert—

“5.
(1)

A cannabis based product for medicinal use in humans.

(2)

A product which is—

(a)

specified in Part 1 as a consequence of the application of paragraphs 2 to 5 of Part 1 to a preparation or other product (not being the substance specified in paragraph 4 of Part 2) which is or contains cannabis, cannabis resin, cannabinol or a cannabinol derivative (not being dronabinol or its stereoisomers ); and

(b)

produced for medicinal use in humans.

(3)

In this paragraph—

  • “cannabis based product for medicinal use in humans” means a preparation or other product (not being the substance specified in paragraph 4 of Part 2), which—

    1. (a)

      is or contains cannabis, cannabis resin, cannabinol or a cannabinol derivative (not being dronabinol or its stereoisomers);

    2. (b)

      is produced for medicinal use in humans; and

    3. (c)

      is—

      1. (i)

        a medicinal product, or

      2. (ii)

        a substance or preparation for use as an ingredient of, or in the production of an ingredient of, a medicinal product; and

  • “medicinal product” has the same meaning as in the Human Medicines Regulations 2012f3.

(4)

In this Schedule “dronabinol” does not include any substance which—

(a)

has the international non-proprietary name dronabinol (recommended by the World Health Organisation); and

(b)

is derived from cannabis, cannabis resin or their constituents,

and stereoisomers of dronabinol are to be construed accordingly.”.

Signature

Sealed with the Official Seal of the Department of Health on 11th October 2018

L.S.

Dr Mark Timoney

A senior officer of the

Department of Health

Explanatory note

(This note is not part of the Order)

Section 7(3) of the Misuse of Drugs Act 1971 (c.38) (the 1971 Act) requires regulations to be made to allow the use for certain purposes, including medical use, of the drugs which are subject to control under that Act. Section 7(4)(b) of the 1971 Act provides, however, that designated controlled drugs will be exempt from this easement and so cannot lawfully be prescribed, administered, produced, compounded or supplied except under licence or other authority issued by the Department of Health. The designations in question are in the Misuse of Drugs (Designation) Order (Northern Ireland) 2001 (the 2001 Order) and include cannabis, cannabis resin, cannabinol and cannabinol derivatives not being dronabinol or its stereoisomers. Article 2 varies the 2001 Order to exclude cannabis based products for medicinal use in humans, and some related products, from the relevant designations.