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Data, Freedom of Information releases and corporate reports
Submissions related to human medicines need to be submitted directly to the MHRA.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Check the tariff classification for vitamin gummies.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Advice on writing clear notices and maximising replies to your FSNs.
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Disciplinary procedures your employer has at work - disciplinary hearings, appeals, suspension, dismissal and help and advice
What happens if you’re suspected of benefit fraud - benefits that can and cannot be stopped if you commit fraud
Information for patients, healthcare professionals and developers of new medicines
Population screening programmes can cause harms as well as benefits, which need to be weighed up by the UK National Screening Committee (UK NSC).
Check what side effects people have reported when they've taken a medicine.
AnimalBiome product seized at East Midlands Airport.
Form ST1: Statement of truth in support of an application for registration based upon adverse possession.
The review of the safety of isotretinoin has concluded.
Information to support your recovery after COVID-19.
Application form ADV1: registration of a person in adverse possession.
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