MHRA-GMDP contains information relating to manufacturing and wholesale distribution authorisations, API registrations and GMP/GDP certificates.

The MHRA products website allows you to find: The leaflets which are provided with medicines; The description of the medicinal product’s properties and how it can be used; Scientific reports about marketing authorisations for medicines; You can look for any word, phrase or Product Licence number (PL) using the search tool.

Registration of manufacturers, importers and distributors of active substances for human use located in the UK. Manufacturers, importers and distributors of active substances are required to register their activities with the MHRA.

The MHRA runs the Yellow Card scheme, which collects and monitors information on suspected safety concerns involving healthcare products, like a side effect with a medicine or an adverse medical device incident.

The MHRA public access registration database (PARD) website allows you to find: Registered manufacturers. Registered medical device types

This form has been designed as an aid to determining the fee that will be charged upon the submission of an application to MHRA. Please note that this form is meant as a guide and the actual fee will have to be paid alongside your application. if you do have any questions please contact [email protected]

The MHRA site for reporting side effects to medicines, vaccines or medical device and diagnostic adverse incidents used in coronavirus treatment

Report a side effect with a medicine or medical device. Make a report. Loading results for ...

The Yellow Card scheme is run by the Medicines and Healthcare products Regulatory Agency (MHRA), which safeguards medical products quality and efficacy in the United Kingdom. Reporting makes a big difference. Your Yellow Card report plays a …

Reporting suspected side effects acts as an early warning system to help the MHRA monitor the safety of medicines through effective regulation. You can read about recognised side effects in the patient information leaflet supplied with a medicine. See our guidance on what to report.