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Statutory Rules of Northern Ireland
HEALTH AND PERSONAL SOCIAL SERVICES
Made
8th March 2002
Coming into operation
1st April 2002
The Department of Health, Social Services and Public Safety(1) in exercise of the powers conferred on it by Articles 56, 63(1), (2), (2A) to (2D), 64, 106(b) and 107(6) of the Health and Personal Social Services (Northern Ireland) Order 1972(2) and of all other powers enabling it in that behalf, and in conjunction with the Department of Finance and Personnel and after consultation with such organisations as appear to the Department of Health, Social Services and Public Safety to be representative of the medical and pharmaceutical professions as required by Articles 56(5) and 63(3) of that Order, hereby makes the following Regulations:
1.—(1) These Regulations may be cited as the Pharmaceutical Services and General Medical Services (Amendment) Regulations (Northern Ireland) 2002 and shall come into operation on 1st April 2002.
(2) In these Regulations—
(a)“the Pharmaceutical Regulations” means the Pharmaceutical Services Regulations (Northern Ireland) 1997(3);
(b)“the Medical Regulations” means the General Medical Services Regulations (Northern Ireland) 1997(4).
2.—(1) Regulation 2 of the Pharmaceutical Regulations (interpretation) is amended as follows.
(2) In paragraph (1)—
(a)in the appropriate alphabetical position insert—
““restricted availability appliance” means an appliance which is approved for particular categories of persons or particular purposes only;”.
3. In regulation 7 of the Pharmaceutical Regulations (removal from pharmaceutical list) paragraph (5)(5) shall be renumbered paragraph (4A).
4. In regulation 9 of the Pharmaceutical Regulations (standards of, and payments for, drugs and appliances), in sub-paragraph (1)(a), at the end, insert “and in the case of a restricted availability appliance, the categories of persons for whom or purposes for which the appliance is approved”.
5. In regulation 11 of the Pharmaceutical Regulations (provision of pharmaceutical services for immediate treatment or personal administration) after sub-paragraph (b) insert “but shall, in either case, provide a restricted availability appliance only if it is for a person or a purpose specified in the Drug Tariff.”.
6. In Schedule 2 of the Pharmaceutical Regulations (terms of service for chemists)—
(a)in paragraph 2 (provision of pharmaceutical services)—
(i)in sub-paragraph 1(a), after “or appliances” insert “not being restricted availability appliances,”;
(ii)after sub-paragraph 1(b), insert—
“(bb)an order for a restricted availability appliance, signed by and endorsed on its face with the reference “S11” by a doctor; or”;
(iii)in sub-paragraph 1(d) after “listed appliances,” insert “not being restricted availability appliances,”; and
(iv)after sub-paragraph 1(d) insert—
“or
(e)an order for a restricted availability appliance, signed by and endorsed on its face with the reference “S11” by a nurse prescriber,”
(b)in paragraph 13—
(i)in sub-paragraph (b), delete “and”;
(ii)in sub-paragraph (c), at the end, insert “; and,”; and
(iii)after sub-paragraph (c), insert—
“(d)he shall provide for the patient a restricted availability appliance only if the patient is a person or it is for a purpose specified in the Drug Tariff.”;
(c)in paragraph 14(2), after “nurse prescriber,” insert “or an order for a restricted availability appliance, signed by and endorsed on its face with the reference “S11” by a nurse prescriber,”;
(d)in paragraph 15(2), after “in this paragraph”, insert “or paragraph 13” and, after “a scheduled drug”, insert “or a restricted availability appliance”.
7.—(1) Schedule 2 to the Medical Regulations (terms of service for doctors) is amended as follows.
(2) In paragraph 1 (interpretation) after the definition of “prescription form” insert—
“restricted availability appliance” means an appliance which is approved for particular categories of persons or particular purposes only;”
(3) In paragraph 48(5) omit the words “or an appliance” and after that sub-paragraph add—
“(6) In the case of urgency a doctor may request a chemist to dispense an appliance before a prescription form is issued only if—
(a)that appliance does not contain a controlled drug within the meaning of the Misuse of Drugs Act 1971(6), other than a drug which is for the time being specified in Schedule 5 to the Misuse of Drugs Regulations (Northern Ireland) 2002(7);
(b)in the case of a restricted availability appliance, the patient is a person, or it is for a purpose, specified in the Drug Tariff; and
(c)he undertakes to furnish the chemist, within 72 hours, with a prescription completed in accordance with sub-paragraph (2).”.
(4) After paragraph 49(2), add—
“(3) In the course of treating such a patient a doctor shall not order on a prescription form a restricted availability appliance unless—
(a)the patient is a person, or it is for a purpose, specified in the Drug Tariff; and
(b)the doctor endorses the face of the form with the reference “S11”,
but may otherwise prescribe such an appliance for that patient in the course of that treatment.”.
Sealed with the Official Seal of the Department of Health, Social Services and Public Safety on 8th March 2002.
L.S.
D. J. Thompson
A senior officer of the
Department of Health, Social Services and Public Safety
Sealed with the Official Seal of the Department of Finance and Personnel on 8th March 2002.
L.S.
Rodney Scott
A senior officer of the
Department of Finance and Personnel
(This note is not part of the Regulations.)
These Regulations further amend the Pharmaceutical Services Regulations (Northern Ireland) 1997, and the General Medical Services Regulations (Northern Ireland) 1997 to take account of the fact that certain appliances may be available for prescription within the Health Services only in circumstances specified by the Department of Health, Social Services and Public Safety.
See S.I. 1999/283 (N.I. 1) Article 3(6)
S.I. 1972/1265 (N.I. 14) relevant amending instruments are S.I. 1978/1907 (N.I. 26) Articles 12 and 14; S.I. 1986/2023 (N.I. 20) Articles 5(1) and (2); S.I. 1986/2229 (N.I. 24) Article 7; S.I. 1988/2249 (N.I. 24) Article 4(5); S.I. 1991/194 (N.I. 1) Articles 29(1), 31(1) and (2) and Schedule 6; section 4 of, and paragraph 30(a) and (b) of the Schedule to 1995 c. 51; S.I. 1992/2671 (N.I. 18) Article 3 and S.I. 1997/1177(N.I. 7) Articles 29 and 32, and Schedule 2
S.R. 1997 No. 381; relevant amending instruments are S.R. 1997 No. 547, S.R. 1998 No. 95, S.R. 1999 Nos. 100 and 254 and S.R. 2001 No. 222
S.R. 1997 No. 380 to which there are amendments not relevant to these Regulations
Paragraph (5) was inserted by S.R. 2001 No. 222
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