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 ...

Professionals have the opportunity to enhance their knowledge on the complex regulatory changes under the MDR and IVDR, gain insights into future developments, and understand their impact on market ...

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 ...

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" ...

Already highly regulated with a risk-based approach at their core, AI-powered medical devices and in vitro diagnostic medical devices face new regulatory constraints stemming from the EU AI Act, a ...

(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" ...