By Dr. Hatem Rabeh · Published August 4, 2026 · Updated August 5, 2026
RAPS workshop for clinical affairs, regulatory and quality professionals on performance studies under the EU IVDR. 2 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).