The Medicines for Human Use (Clinical Trials) (Amendment) Regulations 2025
Write the words of this act the way you think they should read. Solon shows your change as a redline against the published text and pins it to that exact text, so it can never be applied to wording you did not see.
Change 1
37 Amendment to Schedule 1
(1) Schedule 1 (conditions and principles of good clinical practice and for the protection of clinical trial subjects) is amended as follows. (2) In the heading, for “subjects” substitute “participants”. (3) In Part 1 (application and interpretation)— (a) for “any subject”, in each place where it occurs, substitute “any participant”; (b) for “that subject”, in each place where it occurs, substitute “that participant”; (c) for “a subject”, in each place where it occurs, substitute “a participant”; (d) in paragraph 1(7)— (i) for “the subject” substitute “the participant”; (ii) omit “or by an appeal panel appointed under Schedule 4”; (e) in paragraph 2, in the definition of “Declaration of Helsinki” omit “, as amended by the General Assembly of the Association in October 1975, October 1983, September 1989 and October 1996”; (f) in paragraph 3— (i) in sub-paragraph (1)— (aa) at the beginning, insert “Subject to sub-paragraph (3),”; (bb) in paragraph (b)(ii), for “given orally” substitute “communicated (whether by talking, using sign language or any other means); (ii) after sub-paragraph (2), insert— (3) Where sub-paragraph (4) applies, the protocol for the clinical trial for which consent is given may make provision for simplified arrangements for obtaining and evidencing consent, which shall include— (a) the reason for obtaining consent using simplified arrangements; (b) the information to be provided to the participant, and the means of providing that information; and (c) the means by which consent shall be evidenced. (4) This sub-paragraph applies where— (a) the investigational medicinal product or, if there is more than one, each of the investigational medicinal products, is authorised for use in the United Kingdom and is used in accordance with that authorisation; (b) the investigational medicinal product or, if there is more than one, each of the investigational medicinal products, is given to the participant in the course of that participant’s routine health care; and (c) the participant receives no additional medication and undergoes no additional intervention or diagnostic procedure, solely for the purposes of the clinical trial. (5) For the purposes of sub-paragraph (4)— “intervention” includes complementary or alternative therapies, the taking of tissue samples, and requirements in relation to imaging and radiotherapy; and “medication” includes nutritional products and alternative remedies. . (4) For Part 2 (conditions and principles which apply to all clinical trials) substitute— Part 2 CONDITIONS AND PRINCIPLES WHICH APPLY TO ALL CLINICAL TRIALS 1 Clinical trials must be conducted in accordance with the principles of good clinical practice set out in the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Guideline for Good Clinical Practice, as amended from time to time. 2 Except where it would be a contravention of these Regulations, clinical trials must be conducted in accordance with the principles of the Declaration of Helsinki. 3 The investigator and sponsor must have regard to all relevant guidance with respect to commencing and conducting a clinical trial. 4 Provision must be made for insurance or indemnity to cover all liabilities of the investigator and sponsor which may arise in relation to the clinical trial. . (5) In Part 3 (conditions which apply in relation to an adult able to consent or who has given consent prior to the onset of incapacity), for “the subject”, in each place where it occurs, substitute “the participant”. (6) In Part 5 (conditions and principles which apply in relation to an incapacitated adult)— (a) for “the subject”, in each place where it occurs, substitute “the participant”; (b) in paragraph 1, for “the subject’s” substitute “the participant’s”; (c) in paragraph 7, for “a subject” substitute “a participant”.
37 Amendment to Schedule 1
(1) Schedule 1 (conditions and principles of good clinical practice and for the protection of clinical trial subjects) is amended as follows. (2) In the heading, for “subjects” substitute “participants”. (3) In Part 1 (application and interpretation)— (a) for “any subject”, in each place where it occurs, substitute “any participant”; (b) for “that subject”, in each place where it occurs, substitute “that participant”; (c) for “a subject”, in each place where it occurs, substitute “a participant”; (d) in paragraph 1(7)— (i) for “the subject” substitute “the participant”; (ii) omit “or by an appeal panel appointed under Schedule 4”; (e) in paragraph 2, in the definition of “Declaration of Helsinki” omit “, as amended by the General Assembly of the Association in October 1975, October 1983, September 1989 and October 1996”; (f) in paragraph 3— (i) in sub-paragraph (1)— (aa) at the beginning, insert “Subject to sub-paragraph (3),”; (bb) in paragraph (b)(ii), for “given orally” substitute “communicated (whether by talking, using sign language or any other means); (ii) after sub-paragraph (2), insert— (3) Where sub-paragraph (4) applies, the protocol for the clinical trial for which consent is given may make provision for simplified arrangements for obtaining and evidencing consent, which shall include— (a) the reason for obtaining consent using simplified arrangements; (b) the information to be provided to the participant, and the means of providing that information; and (c) the means by which consent shall be evidenced. (4) This sub-paragraph applies where— (a) the investigational medicinal product or, if there is more than one, each of the investigational medicinal products, is authorised for use in the United Kingdom and is used in accordance with that authorisation; (b) the investigational medicinal product or, if there is more than one, each of the investigational medicinal products, is given to the participant in the course of that participant’s routine health care; and (c) the participant receives no additional medication and undergoes no additional intervention or diagnostic procedure, solely for the purposes of the clinical trial. (5) For the purposes of sub-paragraph (4)— “intervention” includes complementary or alternative therapies, the taking of tissue samples, and requirements in relation to imaging and radiotherapy; and “medication” includes nutritional products and alternative remedies. . (4) For Part 2 (conditions and principles which apply to all clinical trials) substitute— Part 2 CONDITIONS AND PRINCIPLES WHICH APPLY TO ALL CLINICAL TRIALS 1 Clinical trials must be conducted in accordance with the principles of good clinical practice set out in the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Guideline for Good Clinical Practice, as amended from time to time. 2 Except where it would be a contravention of these Regulations, clinical trials must be conducted in accordance with the principles of the Declaration of Helsinki. 3 The investigator and sponsor must have regard to all relevant guidance with respect to commencing and conducting a clinical trial. 4 Provision must be made for insurance or indemnity to cover all liabilities of the investigator and sponsor which may arise in relation to the clinical trial. . (5) In Part 3 (conditions which apply in relation to an adult able to consent or who has given consent prior to the onset of incapacity), for “the subject”, in each place where it occurs, substitute “the participant”. (6) In Part 5 (conditions and principles which apply in relation to an incapacitated adult)— (a) for “the subject”, in each place where it occurs, substitute “the participant”; (b) in paragraph 1, for “the subject’s” substitute “the participant’s”; (c) in paragraph 7, for “a subject” substitute “a participant”.
One line that says what changes, such as "Halve the dog tax".
Who it helps, what it costs, what it fixes. It is what persuades people to support it.
A proposal here is not law. Support on Solon is evidence that people want the change; the official route says what it takes to make it law.
Sign in to file your proposal. What you have written stays on this page.
Sign in to file itThink it through
Ask what your change would do, who would gain and who would bear a cost, and where something like it is already law. The assistant reads your draft as it stands, cites the law and the studies it finds, and takes no side. What you file stays yours.