Summary of the latest safety advice for medicines and medical device users
Similar Posts
Designated standards prioritisation
The MHRA invite feedback on the use of designated standards for medical devices and in vitro diagnostic (IVD) devices to help shape future initiatives.
MHRA Safety Roundup: June 2025
Summary of the latest safety advice for medicines and medical device users
100 years of protecting patients through biological standards for medicines
The MHRA produces over 95 per cent of the World Health Organization’s (WHO) biological standards.
Medicines: apply for a variation to your marketing authorisation
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Field Safety Notices: 09-13 February 2026
A list of Field Safety Notices: 09-13 February 2026
Guidance: International Recognition Procedure
How to use the procedure for medicines licensing applications.