The European Court of Justice on Friday ruled that carmakers like Volkswagen remain liable for using unlawful defeat devices, ...

[7] Gail A. Van Norman, Drugs, devices, and the FDA: Part 2: An Overview of Approval Processes: FDA Approval of Medical Devices, 1 JACC: Basic to Translational Science 277, 277, 283 (2016).

DUBLIN--(BUSINESS WIRE)--The "European Handbook of Medical Devices Regulatory Affairs 2019" directory has been added to ResearchAndMarkets.com's offering. As medical device quality assurance and ...

Contract Regulatory Affairs Management Market for Medical Devices, 2019-2030 - ResearchAndMarkets.com January 03, 2020 10:29 AM Eastern Standard Time ...

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 ...

The advent of artificial intelligence (AI) and data-driven methodologies has triggered a wave of transformation in regulatory compliance and quality assurance for the development of medical ...

The European Union''s Medical Device Regulation (MDR) is a complex regulatory framework created to put in place rules and requirements in how medical devices are designed, manufactured, and marketed.

That's in part because of a regulatory review process known as 510 (k) for a section of the FDA law covering medical devices. Manufacturers typically show their product has "substantial ...

The India-UK trade pact has incorporated a mutual recognition agreement framework to facilitate smoother entry of medical ...

The Nigerian Midstream and Downstream Petroleum Regulatory Authority (NMDPRA) has recommended stricter measures for fuel ...