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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.
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.
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)
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.
Decentralised Manufacturing Master File (DMMF) template to be completed for a product specific DMMF document.
Form to apply for a blood establishment authorisation and guidance on completing the form.
Forms to apply for or to make a variation to a manufacturer licence (MANA) or manufacturer ‘specials’ licence for veterinary medicines (MANSA).
Application Form to be completed by an Applicant and sent to the MHRA requesting consideration of an award of a Decentralised Manufacture (DM) Designation.
Report a website or online seller to the MHRA if you think they’re offering medicines or medical devices illegally.
This leaflet outlines the lessons learnt from reports received on adverse incidents around dialysis.
Forms to make a variation to a Blood establishment Authorisation
Check if a website selling medicines is ‘not recommended’ by the Medicines and Healthcare products Regulatory Agency (MHRA).
Do not include personal or financial information like your National Insurance number or credit card details.
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