
2005 No. 119
DANGEROUS DRUGS
The Misuse of Drugs (Amendment) Regulations (Northern Ireland) 2005
Made 15th March 2005
Coming into operation 11th April 2005
The Department of Health, Social Services and Public Safety in exercise of the powers conferred upon it by sections 7, 10, 22 and 31 of the Misuse of Drugs Act 1971, as adapted by section 38 of that Act and now vested in it and of all other powers enabling it in that behalf and after consultation with the Advisory Council on the Misuse of Drugs in accordance with section 31(3) of that Act, hereby makes the following Regulations:
Citation and commencement
1 
These Regulations may be cited as the Misuse of Drugs (Amendment) Regulations (Northern Ireland) 2005 and shall come into operation on 11th April 2005.
Interpretation
2 
The Interpretation Act (Northern Ireland) 1954 shall apply to these Regulations as it applies to an Act of the Northern Ireland Assembly.
Amendment of the Misuse of Drugs Regulations (Northern Ireland) 2002
3 

(1) The Misuse of Drugs Regulations (Northern Ireland) 2002 shall be amended as follows.
(2) In regulation 2(2) –
(a) after the definition of “authorised as a member of a group”, insert ““clinical management plan” has the same meaning as in the Prescription Only Medicines (Human Use) Order 1997;
(b) in the definition of “prescription”, after “prescriber for the medical treatment of a single individual”, insert “by a supplementary prescriber for the medical treatment of a single individual;”;
(c) after the definition of “state registered paramedic”, insert ““supplementary prescriber” has the same meaning as in the Prescription Only Medicines (Human Use) Order 1997”;
(3) In regulation 6(2), after “registered nurse”, insert “, a supplementary prescriber”.
(4) In regulation 6A(2), after “treatment services” insert –“
(d) a supplementary prescriber acting under and in accordance with the terms of a clinical management plan”.
(5) In regulation 7, after paragraph (5) insert –“
(6) Notwithstanding the provisions of paragraph (3), a supplementary prescriber acting under and in accordance with the terms of a clinical management plan may administer to a patient, without the directions of a doctor or dentist, any drug specified in Schedule 2, 3 or 4.
(7) Notwithstanding the provisions of paragraph (3), any person may administer to a patient, in accordance with the directions of a supplementary prescriber acting under and in accordance with the terms of a clinical management plan, any drug specified in Schedule 2, 3 or 4.”
(6) In regulation 8(2), after paragraph (j) insert –“
(k) a supplementary prescriber acting under and in accordance with the terms of a clinical management plan,”.
(7) In regulation 9(2), after paragraph (h) insert –“
(i) a supplementary prescriber acting under and in accordance with the terms of a clinical management plan,”.
(8) In regulation 10 –
(a) in paragraph (1)(a), “(k)” shall be substituted for “(j)”;
(b) in paragraph (1)(b), “(i)” shall be substituted for “(h)”;
(c) in paragraph (2) after “practitioner”, insert “, a supplementary prescriber acting under and in accordance with the terms of a clinical management plan”;
(d) in paragraph (2) after “doctor”, insert “, a supplementary prescriber”;
(e) in paragraph (2)(a) after the first “doctor”, insert “, another supplementary prescriber”;
(f) in paragraph (2)(a) after the second “doctor”, insert “, supplementary prescriber”.
(9) In regulation 14(4) after paragraph (f), insert –“
(g) a supplementary prescriber”.
(10) In regulation 18(2)(d) after “practitioner”, insert “or supplementary prescriber”.
(11) In regulation 26(2) after paragraph (h), insert –“
(i) a supplementary prescriber”.
Sealed with the Official Seal of the Department of Health, Social Services and Public Safety on 15th March 2005.
Deirdre Kenny
A Senior Officer of the
Department of Health, Social Services and Public Safety
