Reference:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 Article 15 (7) - (10): Difference between revisions
From GxPlex
gxplex>GxPlexBot Import from GxPlex Excel |
Gxplex admin (talk | contribs) m 1 revision imported |
||
| (One intermediate revision by one other user not shown) | |||
| Line 1: | Line 1: | ||
{{ | {{ReferenceData | ||
| | |has_document=Document:GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 | ||
| | |module=1 | ||
| | |unit=1.5.4 | ||
|scope=HM | |||
|doc_part=Article 15 | |||
(7) - (10) | (7) - (10) | ||
| | |language=EN | ||
| | |entry_by=Florian Adragna | ||
| | |contributors= | ||
|tags=TAG-00134-Eth-kom ++ TAG-00027-Inc-son ++ TAG-00154-Vul-eil ++ TAG-00029-Inf-rte | |||
|tags_display=[[Glossary:TAG-00134-Eth-kom|Ethics committee]], [[Glossary:TAG-00027-Inc-son|Incapacitated subject]], [[Glossary:TAG-00154-Vul-eil|Vulnerable participants]], [[Glossary:TAG-00029-Inf-rte|Informed consent]] | |||
|comment=Ethics committee opinion: additional conditions for vulnerable subjects | |||
|content=Application for ethics committee opinion | |||
| | |||
| | |||
= | |||
Application for ethics committee opinion | |||
15.— (7) If— | 15.— (7) If— | ||
| Line 66: | Line 35: | ||
(a)in the case of medicinal products for gene therapy or somatic cell therapy, the use of such therapies in the treatment of humans; or | (a)in the case of medicinal products for gene therapy or somatic cell therapy, the use of such therapies in the treatment of humans; or | ||
(b)in the case of medicinal products containing genetically modified organisms, the administration of such products to humans. | (b)in the case of medicinal products containing genetically modified organisms, the administration of such products to humans. | ||
}} | |||
Latest revision as of 13:49, 16 July 2026
| Document information | |
|---|---|
| Reference | GBR The Medicines for Human Use (Clinical Trials) Regulations 2004 01-May-2004 |
| Validity area | GBR |
| Scope(s) | HM |
| Document name | The Medicines for Human Use (Clinical Trials) Regulations 2004 |
| Version / Revision | 01-May-2004 |
| Status | Current |
| Document type | Legal act |
| Language(s) | EN |
| Description | The Medicines for Human Use (Clinical Trials) Regulations 2004 |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 1 — Unit 1.5.4 |
| Scope | HM |
| Document part | Article 15
(7) - (10) |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Ethics committee, Incapacitated subject, Vulnerable participants, Informed consent |
Content
Application for ethics committee opinion 15.— (7) If—
(a)any subject to the clinical trial is to be an adult incapable by reason of physical and mental incapacity to give informed consent to participation in the trial; and (b)the committee does not have a member with professional expertise in the treatment of— (i)the disease to which the trial relates, and (ii)the patient population suffering that disease,it shall, before giving its opinion, obtain advice on the clinical, ethical and pyschosocial problems in the field of that disease and patient population which may arise in relation to that trial. (8) The ethics committee shall consider, and give an opinion on, any other issue relating to the clinical trial, if—
(a)the committee has been asked by the applicant to consider the issue; (b)it is, in the committee’s opinion, relevant to the other matters considered by the committee in accordance with this regulation. (9) Where an ethics committee gives an opinion in accordance with this regulation, it shall publish a summary of that opinion.
(10) In this regulation—
“the specified period” means— (a)in the case of a clinical trial involving a medicinal product for gene therapy or somatic cell therapy or a medicinal product containing a genetically modified organism— (i)where a specialist group or committee is consulted, 180 days, or (ii)where there is no such consultation, 90 days; or (b)in any other case, 60 days; “specialist group or committee” means a group or committee whose functions include the provision of advice on ethical or scientific issues in relation to— (a)in the case of medicinal products for gene therapy or somatic cell therapy, the use of such therapies in the treatment of humans; or (b)in the case of medicinal products containing genetically modified organisms, the administration of such products to humans.
