MHRA Final Rules for Post-Market Surveillance
Medicines and Healthcare Products Regulatory Agency (MHRA) finaliz...
Medical Devices – USA/Europe/Asia Regulatory Updates Roundup, Oct 2023
USA | EUROPE | ASIA
USA Guiding Principles on Predetermined Change...
UK MHRA Extending Acceptance of CE Devices
The Medicines & Healthcare products Regulatory Agency (MHRA), ...
Adverse Event Reporting in UK – SaMD
Any event which meets these three reporting criteria is considered...
Medical Devices – USA/Europe/Asia Regulatory Updates Roundup, Feb 2023
USA (FDA) | CANADA (HC) | EUROPE | SWITZERLAND (Swissmedic) | FINL...
BioPharma – USA/Europe Regulatory Updates, Week 2 Nov 2022
Europe (EU) | USA | Asia
Europe (EU) EMA consults on planned updat...
