Latest News from ACDM
Have your say – MHRA’s public consultation on proposals for legislative changes for clinical trials
January 26, 2022
We have just launched our 8-week public consultation on proposals for legislative changes for clinical trials.
We want to streamline clinical trial approvals, enable innovation, enhance clinical trials transparency, enable greater risk proportionality, and promote patient and public involvement in clinical trials.
We would like to hear from clinical trial participants, researchers, developers, manufacturers, sponsors, investigators, healthcare professionals and the wider public to help shape improvements to the legislation for clinical trials.
You can read more about our proposals in our Press release and consultation document.
Please do share this email and the social media links below with your networks and contacts so that we can get the broadest possible response.
The consultation will close at 11pm on Monday, 14 March 2022.
Thank you for your support.
The Medicines and Healthcare products Regulatory Agency
ACDM Comments on “Digital Health Technologies for Remote Data Acquisition in Clinical Investigations; Draft Guidance for Industry, Investigators, and Other Stakeholders; Availability” April 5, 2022
ICH E8 (R1) General Considerations for Clinical Studies Impact on Data Management April 5, 2022
Have your say – MHRA’s public consultation on proposals for legislative changes for clinical trials January 26, 2022
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