Navigate opportunities in the evolving EU and UK medical device markets by understanding the MDR/IVDR regulations. Gain insights into UK regulatory changes, anticipate future digital medicine ...
The introduction of new Post-Market Surveillance regulations and UKCA marking processes presents key opportunities for medical device manufacturers to align compliance strategies and enhance market ...
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" ...
DONGGUAN, GUANGDONG, CHINA, January 22, 2026 /EINPresswire.com/ — As global healthcare systems increasingly emphasize ...
The "Medical Device Regulations in the Middle East and North Africa Training Course (May 18th - May 19th, 2026)" has been added to ResearchAndMarkets.com's offering. The size of the medical device ...
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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