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 ...

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, Dec. 23, 2025 (GLOBE NEWSWIRE) -- The "Medical Device Regulations in Asia-Pacific Markets Training Course (Mar 3rd - Mar 4th, 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" ...

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 ...

The "Navigating Regulatory Compliance Whilst Developing and Distributing Polymerase Chain Reaction (PCR)-Based IVD Tests Training Course (May 15, 2026)" has been added to ResearchAndMarkets.com's ...

The Elena and Miles Zaremski Law Medicine Forum presents: Medical Device Regulation: Going from Bad to Worse...or Better? with George Horvath Innovations in medical device technology hold the ...

State licensing for prescription medical device manufacturers and distributors is a complex and evolving landscape. While FDA oversees federal regulations, individual states impose their own licensing ...

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" ...

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 ...