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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
How to get information including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
MHRA updates product information regarding the very rare risk of non-arteritic anterior ischemic optic neuropathy (NAION) in patients taking semaglutide.
We deal with complaints about cases where a company name is registered for the primary purpose of preventing someone else with legitimate interest from registering it, or demanding payment from them to release it. Company Names Tribunal works with the...
Guidance on labelling for medicinal products used in clinical trials.
Decision for applicant Day Lewis Plc registration number 16240749, applicant successful.
List of words and phrases that will cause a veterinary product to be medicinal by presentation either through use or contextual use.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Minutes of meetings held between government, NHS England and the ABPI to review the operation of the 2019 voluntary scheme for branded medicines pricing and access.
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