By Dr. Hatem Rabeh · Published August 4, 2026 · Updated August 5, 2026
RAPS workshop on implementing the EU MDR, covering quality system updates and oversight of economic operators. 12 CE credits.
Event details and registration
Dates are those published by the organiser. Confirm on the organiser’s page before booking travel.
The comprehensive free database for medical device companies, FDA-cleared devices, EU Notified Bodies, competent authorities, clinical guidelines, and regulatory resources worldwide - 4,975 companies · 5,064 devices · 53 EU Notified Bodies · 1,129 resources & guidelines. Founded by Dr. Hatem Rabeh (MD, MSc Ing).