Medical Devices – Regulatory Updates – August Volume 2
EUROPE
1. Guidance on MHRA’s Return to On‑Site Inspections
With the easing of COVID‑19 restrictions, the MHRA inspectorate will begin resuming on‑site, risk‑based GxP inspections in...
EU Medical Device Labelling, Europe medical devices regulatory updates, India dgft regulatory updates, Medical device labelling requirements, Medical Devices Regulatory Updates, Regulatory Updates August Volume 2, us medical devices regulatory updates