Before placing a medical device on the European market, manufacturers need to produce technical documentation providing evidence of conformity with the relevant legislation. From the 26 May 2020, ...
Dublin, April 06, 2023 (GLOBE NEWSWIRE) -- The "The DHF, DMR, DHR, EU MDR Technical Documentation Similarities, Differences and The Future" training has been added to ResearchAndMarkets.com's offering ...
The European Commission’s Medical Device Coordinating Group (MDCG) has revised several documents addressing the ...
Notified body trade group Team-NB has revised its best practice guidance for submitting technical documentation under Annex II and II of the Medical Device Regulation (MDR). The European Association ...
After a shove from European Parliament, EU member states, and industry stakeholders, the European Commission (EC) issued ...
Dublin, July 30, 2025 (GLOBE NEWSWIRE) -- The "Advanced Regulatory Affairs for Medical Devices Training Course" training has been added to ResearchAndMarkets.com's offering. Explore the MDR's updates ...
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