Dublin, March 25, 2025 (GLOBE NEWSWIRE) -- The "Global Handbook of Medical Devices Regulatory Affairs 2025" directory has been added to ResearchAndMarkets.com's offering. Medical device regulation ...
Evolving regulations and market requirements have kept medtech companies on their toes for years. EU MDR, for example, has ...
The European Society of Cardiology (ESC) has urged the European Commission to revise the Medical Device Regulation (EU ...
Medical device manufacturers and distributors have come under increasing scrutiny from state licensing agencies and operating without a ...
Switzerland is working toward reestablishing its relationship with the EU while exploring new avenues. Meanwhile, the U.K. is ...
Manufacturers are turning to consultancies specialising in medical device regulatory affairs for their UKRP needs, as these can typically grant access to an entire team of specialists and offer ...
The "Medical Device Studies: Regulatory Requirements and Adverse Event Reporting Training Course" has been added to ResearchAndMarkets.com's offering. This seminar provides an essential overview of ...
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