This week in Pedersen's POV, our senior editor finds humor in the European Commmission's plan to simplify the EU Medical ...

If finalized, the changes would reduce the scope of AI regulations for medical devices and include more provisions for rare ...

Following the identification of several key challenges in the application of the Medical Device Regulation (MDR) and In Vitro ...

Since the 2017 publication of the medical device regulation (MDR) and the IVD regulation (IVDR), EU regulations for medical ...

Health ministry issues draft notification with various amendments in MDR, 2017: Gireesh Babu, New Delhi Thursday, December 18, 2025, 08:00 Hrs [IST] The Union health ministry has ...

DUBLIN--(BUSINESS WIRE)--The "Medical Device Software: Complying with the EU MDR, EU IVDR & FDA Regulations" conference has been added to ResearchAndMarkets.com's offering. This intensive four-day ...

LE MONT-SUR LAUSANNE, Switzerland--(BUSINESS WIRE)--Regen Lab, a global commercial-stage medical technology company specializing in the research, development, registration, manufacturing and ...

The Central Drugs Standard Control Organisation (CDSCO) has launched a new risk classification module on the drug regulator's online system for medical devices in order to simplify the regulatory ...