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 ...

Designing medical devices for such varied use cases requires more than just technical proficiency. It calls for strategic ...

A clear intellectual property and product risk evaluation strategy helps device companies with investments and M&A.

[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).

Guwahati: National Institute of Pharmaceutical Education and Research (NIPER), Guwahati has announced the launch of a ...

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 ...

In this hoganlovells.com Q&A, Hogan Lovells counsel Fabien Roy addresses EU regulations that apply to medical devices that are produced using 3-D printing technologies. In 2015, the UK ...