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Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Apply for a public health exemption from the sunset clause.
Check what side effects people have reported when they've taken a medicine.
Forms to make a variation to a manufacturer's licence.
To apply for a manufacturer licence, complete the appropriate form. Applications for a manufacturer licence will be payable on invoice.
Download MHRA's Request for Further Information (RFI) response template, with guidance on how to complete it.
Check if someone selling medicines online in Northern Ireland is allowed to do so by the Medicines and Healthcare products Regulatory Agency (MHRA)
Notification form to confirm the import is requested by a doctor or dentist and is for use by his patients on his direct responsibility.
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
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).
Template for a blood bank compliance report and guidance on completing it.
This leaflet outlines the lessons learnt from reports received on adverse incidents around dialysis.
Renew your marketing authorisation for one or more human or veterinary medicinal products.
Form to apply for a blood establishment authorisation and guidance on completing the form.
Forms to make a variation to a Blood establishment Authorisation
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