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