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
16 Substitution of regulation 27B
For regulation 27B (publication of information) substitute— Publication of information 27B (1) Subject to paragraph (3), the Authority may make accessible to the public information contained in the items listed in paragraph (2) insofar as it relates to a clinical trial carried out, or being carried out, under these Regulations. (2) The items listed in this paragraph are— (a) the request for approval made under regulation 16; (b) any amended request for approval made under regulation 18A; (c) any substantial modification to the clinical trial approval made under regulation 21, 22, 22A or 22B; (d) the favourable opinion of the ethics committee given in accordance with regulation 18(1)(b); (e) the notification of the end of the clinical trial made under regulation 27. (3) Prior to making information available to the public under paragraph (1), the Authority must, after consulting such persons as they consider appropriate, publish a list of the information which may be made accessible to the public under paragraph (1). .
16 Substitution of regulation 27B
For regulation 27B (publication of information) substitute— Publication of information 27B (1) Subject to paragraph (3), the Authority may make accessible to the public information contained in the items listed in paragraph (2) insofar as it relates to a clinical trial carried out, or being carried out, under these Regulations. (2) The items listed in this paragraph are— (a) the request for approval made under regulation 16; (b) any amended request for approval made under regulation 18A; (c) any substantial modification to the clinical trial approval made under regulation 21, 22, 22A or 22B; (d) the favourable opinion of the ethics committee given in accordance with regulation 18(1)(b); (e) the notification of the end of the clinical trial made under regulation 27. (3) Prior to making information available to the public under paragraph (1), the Authority must, after consulting such persons as they consider appropriate, publish a list of the information which may be made accessible to the public under paragraph (1). .
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.
How this law is officially changed
Solon does not know this law's official route yet. The proposal is recorded all the same, and the route appears here once its source is added.
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.