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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 have taken a medicine.
Forms to make a variation to a manufacturer's licence.
Download MHRA's Request for Further Information (RFI) response template, with guidance on how to complete it.
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)
Apply for a public health exemption from the sunset clause.
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
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.
Form to apply for a blood establishment authorisation and guidance on completing the form.
Renew your marketing authorisation for one or more human or veterinary medicinal products.
Forms to make a variation to a Blood establishment Authorisation
Forms to apply for or to make a variation to a manufacturer licence (MANA) or manufacturer ‘specials’ licence for veterinary medicines (MANSA).
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