Dublin, July 30, 2025 (GLOBE NEWSWIRE) -- The "Advanced Regulatory Affairs for Medical Devices Training Course" training has been added to ResearchAndMarkets.com's offering. Explore the MDR's updates ...

Dublin, July 15, 2025 (GLOBE NEWSWIRE) -- The "The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) ...

(MENAFN- GlobeNewsWire - Nasdaq) Join our seminar for a comprehensive guide on medical device clinical evaluations, focusing on MDR and adverse event reporting. Ideal for both newcomers and seasoned ...

Dublin, Sept. 24, 2025 (GLOBE NEWSWIRE) -- The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Oct 21, 2025)" training ...

The "An Introduction to the Medical Device Regulation Training Course" conference has been added to ResearchAndMarkets.com's offering. This seminar provides an invaluable overview of the European ...

It’s tough for medical device companies to get that stamp of FDA approval, but the labyrinthine regulatory pathway certainly doesn’t help things. Regulators want to change that: “…we learned that the ...

The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Oct 21, 2025)" training has been added to ResearchAndMarkets.com's ...