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The Medicines for Human Use (Clinical Trials) Regulations 2004, Section 5 is up to date with all changes known to be in force on or before 09 March 2025. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations.
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5.—(1) The body responsible for establishing, recognising and monitoring ethics committees in the United Kingdom in accordance with these Regulations is the United Kingdom Ethics Committees Authority, which is a body consisting of—
(a)[F1the Health Research Authority];
(b)the National Assembly for Wales;
(c)the Scottish Ministers; and
(d)the Department for Health, Social Services and Public Safety for Northern Ireland.
(2) The functions of the Authority—
(a)may, by agreement between them, be performed by any one of [F2the Health Research Authority], the National Assembly for Wales, the Scottish Ministers and the Department for Health, Social Services and Public Safety for Northern Ireland acting alone, or any two or more of them acting jointly; and
(b)may be performed by any one of [F2the Health Research Authority], the National Assembly for Wales, the Scottish Ministers and the Department for Health, Social Services and Public Safety for Northern Ireland acting alone solely in relation to a part of the United Kingdom with respect to which [F3the Health Research Authority], the Assembly, the Ministers or the Department, as the case may be, have responsibilities.
(3) In accordance with the preceding provisions of this regulation, in these Regulations “the United Kingdom Ethics Committees Authority” (“the Authority”) means any one or more of [F4the Health Research Authority], the National Assembly for Wales, the Scottish Ministers and the Department for Health, Social Services and Public Safety for Northern Ireland, and, in the case of anything falling to be done by the Authority, means any one or more of them acting as mentioned in paragraph (2).
(4) The Authority may appoint such persons as they think necessary for the proper discharge by them of their functions, and those persons shall be appointed on such terms and conditions (including conditions as to remuneration, benefits, allowances and reimbursement for expenses) as the Authority think fit.
(5) Arrangements may be made between the Authority and any relevant authority for—
(a)any functions of the Authority to be exercised by, or by members of staff of, the relevant authority; or
(b)the provision of staff, premises or administrative services by the relevant authority to the Authority.
(6) Any arrangements under paragraph (5) for the exercise of any functions of the Authority shall not affect the responsibility of the Authority.
(7) In this regulation, “relevant authority” means any government department, local or public authority or holder of public office.
Textual Amendments
F1Words in reg. 5(1) substituted (1.1.2015) by Care Act 2014 (c. 23), ss. 116(a), 127 (with s. 119(3)); S.I. 2014/2473, art. 5(h)
F2Words in reg. 5(2) substituted (1.1.2015) by Care Act 2014 (c. 23), ss. 116(a), 127 (with s. 119(3)); S.I. 2014/2473, art. 5(h)
F3Words in reg. 5(2) substituted (1.1.2015) by Care Act 2014 (c. 23), ss. 116(b), 127; S.I. 2014/2473, art. 5(h)
F4Words in reg. 5(3) substituted (1.1.2015) by Care Act 2014 (c. 23), ss. 116(a), 127 (with s. 119(3)); S.I. 2014/2473, art. 5(h)
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