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, Feb. 25, 2026 (GLOBE NEWSWIRE) -- The "Medical Device Regulation in the Eurasian Union, Russia and the CIS Training Course (June 30, 2026 and July 1, 2026)" training has been added to ...

"The Role of the Person Responsible for Regulatory Compliance (PRRC) Under the MDR (Medical Device Regulation) and IVDR (In-Vitro Diagnostic Regulation) Training Course (Mar 4, 2026)" has been added ...

The countdown is on for medical device manufacturers to prepare for the EU Regulation on Medical Devices (MDR), which will fully apply in member states from May this year. But in a recently published ...

(MENAFN- GlobeNewsWire - Nasdaq) Key market opportunities include gaining insights into CIS medical device regulations, understanding new EAEU business implications, and clarifying registration ...

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" ...