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Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Check what side effects people have reported when they've taken a medicine.
To apply for a manufacturer licence, complete the appropriate form. Applications for a manufacturer licence will be payable on invoice.
Check if someone selling medicines online in Northern Ireland is allowed to do so by the Medicines and Healthcare products Regulatory Agency (MHRA)
Forms to make a variation to a manufacturer's licence.
Apply for a public health exemption from the sunset clause.
Download MHRA's Request for Further Information (RFI) response template, with guidance on how to complete it.
Notification form to confirm the import is requested by a doctor or dentist and is for use by their patients on their direct responsibility.
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).
Form to apply for a blood establishment authorisation and guidance on completing the form.
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
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.
Forms to make a variation to a Blood establishment Authorisation
Don’t include personal or financial information like your National Insurance number or credit card details.
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