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Data, Freedom of Information releases and corporate reports
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Check the veterinary product information database to find out if a medicine is safe to use on your pet or has been removed from sale.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines
This holiday season, the MHRA is reminding people that some common festive foods can interact with medicines, altering how well they work or increasing the risk of side effects.
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