The Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008

• Citation: S.I. 2008/941
• Sections: 9

Section 1 Citation, commencement and interpretation

(1) These Regulations may be cited as the Medicines for Human Use (Clinical Trials) and Blood Safety and Quality (Amendment) Regulations 2008 and shall come into force on 1st May 2008.

(2) In these Regulations—

“the Blood Regulations” means the Blood Safety and Quality Regulations 2005 ;

“the Clinical Trials Regulations” means the Medicines for Human Use (Clinical Trials) Regulations 2004 .

Section 2 Amendment of regulation 2 of the Clinical Trials Regulations

In regulation 2 of the Clinical Trials Regulations (interpretation), in paragraph (1)—

(a) for the definition of “the Directive” substitute the following definition—

“ the Directive ” means Directive 2001/20/EC of the European Parliament and of the Council on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use ;

(b) for the definition of “Directive 2001/83/EC ” substitute the following definition—

“ Directive 2001/83/EC ” means Directive 2001/83/EC of the European Parliament and of the Council on the Community code relating to medicinal products for human use ;

(c) in the definition of “the Gene Therapy Advisory Committee” omit the words from “to” to the end.

Section 3 Amendment of regulation 15 of the Clinical Trials Regulations

In regulation 15 of the Clinical Trials Regulations (ethics committee opinion)—

(a) for paragraph (1), substitute the following paragraph—

(1) Except as provided for in paragraph (4A) (which removes the requirement on the Gene Therapy Advisory Committee to give an opinion) and subject to paragraphs (3) and (4) (which suspend and disapply time limits respectively), an ethics committee shall give an opinion in relation to the clinical trial to which a valid application relates within the specified period beginning with the date of receipt of the valid application.

(b) after paragraph (3) insert the following paragraphs—

(3A) An ethics committee may give a favourable opinion subject to conditions specified in writing in relation to a clinical trial.

(3B) If an ethics committee gives a favourable opinion subject to conditions, the ethics committee is to be treated as having given a favourable opinion in relation to the clinical trial only if the specified conditions are satisfied.

(c) after paragraph (4), insert the following paragraphs—

(4A) Where a notification under paragraph (4B) is received by the Authority—

(a) the Gene Therapy Advisory Committee shall not give an opinion in relation to the clinical trial to which the application subject to that notification relates;

(b) the Authority shall direct that the application be considered by another ethics committee specified in the direction;

(c) the Gene Therapy Advisory Committee shall send the application to the ethics committee specified in the direction immediately following the direction being given; and

(d) the ethics committee specified in the direction shall, subject to the application being valid, give an opinion in relation to the clinical trial to which that application relates within the specified period beginning with the date of the Gene Therapy Advisory Committee’s receipt of the application.

(4B) The Chairman, vice-chairman or alternate vice-chairman of the Gene Therapy Advisory Committee may notify the Authority (instead of giving an opinion) within the specified period beginning with the date of the Committee’s receipt of an application that the clinical trial to which that application relates does not merit an opinion from the Gene Therapy Advisory Committee.

Section 4 Amendment of Schedule 1 to the Clinical Trials Regulations

(1) In Schedule 1 to the Clinical Trials Regulations (conditions and principles of good clinical practice and for the protection of clinical trial subjects), in Part 1 (application and interpretation), paragraph 1 shall be amended as follows.

(2) In sub-paragraph (3), for “If” substitute “Subject to sub-paragraphs (6) and (7), if”.

(3) In sub-paragraph (6)—

(a) after “a subject who is” insert “a minor or”; and

(b) for “Part 5” substitute “Part 4 in the case of a minor or paragraphs 1 to 5 of Part 5 in the case of an incapacitated adult”.

(4) In sub-paragraph (7), for “Part 5” substitute “Part 4 in the case of a minor or paragraphs 1 to 5 of Part 5 in the case of an incapacitated adult”.

Section 5 Amendment of Schedule 2 to the Clinical Trials Regulations

(1) Schedule 2 to the Clinical Trials Regulations (additional provisions relating to ethics committees) shall be amended as follows.

(2) In paragraph 1 (interpretation), in the definition of “expert member”, in sub-paragraph (b), for “clinical trials” substitute “clinical research”.

(3) In paragraph 3 (membership), in sub-paragraph (3), for “Subject to paragraph 7, the” substitute “The”.

(4) In paragraph 6 (committees, meetings and proceedings)—

(a) in sub-paragraph (2), for “sub-paragraph (4)” substitute “sub-paragraphs (4) and (4A)”;

(b) for sub-paragraph (4) substitute the following sub-paragraphs—

(4) All valid applications for an ethics committee opinion must be considered by a full meeting of an ethics committee.

(4A) Where a full meeting of an ethics committee has considered a valid application and reached a provisional opinion, it may delegate the final determination of its opinion in accordance with regulation 15 to the Chairman of the ethics committee or a sub-committee of specified members.

(c) after sub-paragraph (5) insert the following sub-paragraph—

(6) For the purposes of this paragraph, a “full meeting of an ethics committee” is one at which at least seven members of the committee (including any members co-opted under paragraph 8) are present, including at least—

(a) one lay member who is not and never has been—

(i) a health care professional, or

(ii) a chairman, member, director, officer or employee of a health service body; and

(b) one expert member.

(5) In paragraph 7 (deputies and co-opted members), in sub-paragraph (1), for “An ethics committee” substitute “The appointing authority”.

(6) In paragraph 8 (co-opted members) —

(a) in sub-paragraph (3) for “an ethics committee” substitute “a committee that advises or has advised on the ethics of research involving human subjects”; and

(b) for sub-paragraph (5) substitute the following sub-paragraph—

(5) A co-opted member shall hold and vacate office in accordance with the ethics committee’s standing orders and operating procedures adopted under paragraph 6(3).

Section 6 Amendment of Schedule 3 to the Clinical Trials Regulations

In Schedule 3 to the Clinical Trials Regulations (particulars and documents), in Part 1 (application for ethics committee opinion), in paragraph 2, for “paragraphs 1 to 4 and 6 to 9” substitute “paragraphs 1 to 3 and 6”.

Section 7 Amendment of regulation 7 of the Blood Regulations

In regulation 8 of the Blood Regulations (labelling of blood and blood components and traceability), in paragraph (3), after “sub-paragraph (a)” insert “of paragraph (2)”.

Section 8 Amendment of regulation 8 of the Blood Regulations

In regulation 9 of the Blood Regulations (hospital blood bank requirements), for sub-paragraph (f) of paragraph 1, substitute—

(f) retain, for a period of at least 15 years, a record of any serious adverse events which may affect the quality or safety of blood and blood components;

Section 9 Amendment of regulation 12B of the Blood Regulations

In regulation 12B of the Blood Regulations (requirement to report serious adverse reactions and events), in paragraph (5), for “(3)(b)” substitute “(4)(b)”.