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The Misuse of Drugs (Amendment) Regulations (Northern Ireland) 2005

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Amendment of the Misuse of Drugs Regulations (Northern Ireland) 2002

3.—(1) The Misuse of Drugs Regulations (Northern Ireland) 2002(1) 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(2);

(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)”;

(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.

(1)

S.R. 2002 No. 1 the relevant amending Regulations are S.R. 2003 Nos. 324 and 420

(2)

S.I. 1997/1830; the definition of “clinical management plan” was inserted by S.I. 2003/696

(3)

S.I. 1997/1830; the definition of “supplementary prescriber” was inserted by S.I. 2003/696 and amended by S.I. 2004/1771

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