The "A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU (European Union) and UK Training Course (Apr 29, 2026)" training has been added to ResearchAndMarkets.com's ...
DUBLIN--(BUSINESS WIRE)--The "The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) Training Course" ...
Key market opportunities include gaining insights into CIS medical device regulations, understanding new EAEU business implications, and clarifying registration procedures. Enhanced knowledge enhances ...
(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 ...
On April 11, AEI’s Brian J. Miller hosted Jesse Ehrenfeld of the American Medical Association and Jeff Shuren of the Food and Drug Administration’s (FDA) Center for Devices and Radiological Health to ...
DUBLIN--(BUSINESS WIRE)--The "Medical Device Regulations in Asia-Pacific Markets Training Course (Nov 3rd - Nov 4th, 2025)" training has been added to ResearchAndMarkets.com's offering. With the ...
DUBLIN--(BUSINESS WIRE)--The "Sterilization of Medical Devices Training Course (Oct 20th - Oct 21st, 2025)" training has been added to ResearchAndMarkets.com's offering. Sterile devices are free of ...
The European Union’s efforts to update its regulatory framework for medical devices was heralded as a long-overdue response to the Poly Implant Prothèse (PIP) breast implant scandal, but the COVID-19 ...
DUBLIN--(BUSINESS WIRE)--The "The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) Training Course" ...
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