Search Legislation

The Misuse of Drugs (Amendment) Regulations (Northern Ireland) 2012

 Help about what version

What Version

  • Latest available (Revised)
  • Original (As made)
 Help about opening options

Opening Options

Status:

This is the original version (as it was originally made). This item of legislation is currently only available in its original format.

EXPLANATORY NOTE

(This note is not part of the Regulations)

These Regulations amend the Misuse of Drugs Regulations (Northern Ireland) 2002 (the “2002 Regulations”) to allow a nurse independent prescriber and a pharmacist independent prescriber (defined in regulation 2(1) of the 2002 Regulations, as amended by regulation 4(b)) to prescribe, possess, supply, offer to supply, administer and give directions for the administration of any controlled drug specified in Schedules 2 to 5 of the 2002 Regulations, but not in relation to cocaine, diamorphine or dipipanone as regards persons addicted to these drugs otherwise than for the purpose of treating organic disease or injury suffered by such persons. The amendments also allow a nurse independent prescriber and a pharmacist independent prescriber to supply certain articles for administering or preparing controlled drugs.

Regulation 8(1)(c) and (d) of the 2002 Regulations (inserted by regulation 10(a)) provides for specified persons to compound any drug specified in Schedule 2 or 5 to the 2002 Regulations for the purposes of administration of that drug in accordance with regulation 7 of the 2002 Regulations, and regulation 9(1)(d) and (e) of the 2002 Regulations (inserted by regulation 11(a)) provides for such compounding in relation to any drug specified in Schedule 3 or 4. Regulation 11(1)(e) of the 2002 Regulations (substituted by regulation 12(b)) allows a person specified in regulations 8(7), 8(8)(a), 9(7) or 9(8) to have in his possession any drug specified in those regulations in accordance with conditions specified in those regulations.

Regulation 13 includes a nurse independent prescriber and a pharmacist independent prescriber within the list of persons in regulation 14(4) of the 2002 Regulations in relation to documentation to be obtained by the supplier of a controlled drug in the circumstances set out in regulation 15. Regulation 14 amends regulation 18 of the 2002 Regulations to the effect that the requirement in regulation 18(1) concerning marking of bottles and other containers does not apply in relation to the supply of a controlled drug by or on the prescription of a nurse independent prescriber or a pharmacist independent prescriber. Regulation 15 amends regulation 26 of the 2002 Regulations to include a nurse independent prescriber within the list of persons in regulation 26(2) in relation to the furnishing of information with respect to controlled drugs.

Regulation 5(a) amends regulation 4(2) of the 2002 Regulations to provide that the application of the provisions referred to in regulation 4(2) are excluded only where a person himself carries out the importation or exportation of the drug specified in Part II of Schedule 4 to the 2002 Regulations. The requirement for such a drug to be contained in a medicinal product is omitted from regulation 4(2) of the 2002 Regulations, as amended by regulation 5(a), and regulations 5(b), 11(a) and (e) and 12(a) make similar amendments. The definition of ‘medicinal product’ is omitted from regulation 2(1) of the 2002 Regulations, as amended by regulation 4(a).

Back to top

Options/Help

Print Options

Close

Legislation is available in different versions:

Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.

Original (As Enacted or Made): The original version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.

Close

Opening Options

Different options to open legislation in order to view more content on screen at once

Close

Explanatory Memorandum

Explanatory Memorandum sets out a brief statement of the purpose of a Statutory Rule and provides information about its policy objective and policy implications. They aim to make the Statutory Rule accessible to readers who are not legally qualified and accompany any Northern Ireland Statutory Rule or Draft Northern Ireland Statutory Rule laid before the UK Parliament during the suspension of the Northern Ireland Assembly.

Close

More Resources

Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as enacted version that was used for the print copy
  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • correction slips
  • links to related legislation and further information resources
Close

More Resources

Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as made version that was used for the print copy
  • correction slips

Click 'View More' or select 'More Resources' tab for additional information including:

  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • links to related legislation and further information resources