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From
Medicines and Healthcare products Regulatory Agency (MHRA)
Find patient information leaflets (PILs) and summaries of product characteristics (SPCs) for different medicines
Check what side effects people have reported when they've taken a medicine.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Find reports by the Medicines and Healthcare products Regulatory Agency (MHRA) approving medicines and vaccines for use in the UK
Check if someone selling medicines online is allowed to do so by the Medicines and Healthcare products Regulatory Agency (MHRA)
To apply for a manufacturer licence, complete the appropriate form.
Forms to make a variation to a manufacturer's licence.
Apply for a public health exemption from the sunset clause.
Notification form to confirm the import is requested by a doctor or dentist and is for use by his patients on his direct responsibility.
Blood facility declaration form to be completed and returned to MHRA.
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
Form to apply for a blood establishment authorisation and guidance on completing the form.
Form to apply for a manufacturer ‘specials’ licence (MS).
Template for a blood bank compliance report and guidance on completing it.
Forms to apply for or to make a variation to a wholesale dealer licence (WDA(V)), manufacturer licence (MANA) or manufacturer ‘specials’ licence for veterinary medicines (MANSA).
Renew your marketing authorisation for one or more human or veterinary medicinal products.
Apply for a traditional herbal registration (THR) to market a traditional herbal medicine (remedy) in the UK.
This leaflet outlines the lessons learnt from reports received on adverse incidents around dialysis.
Forms to make a variation to a Blood establishment Authorisation
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