Dublin, Jan. 17, 2024 (GLOBE NEWSWIRE) -- The "Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) - A Technical Documentation Training" training has been added to ...
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 ...
There are key regulatory documents global medical device companies must meet for the U.S. and the European Union / Common Market. And there are important differences. The cGMPs mandate Design Control ...
(MENAFN- GlobeNewsWire - Nasdaq) The seminar on medical device manufacturing highlights key opportunities in enhancing technical documentation, focusing on the integration of DHF, DMR, and DHR. It ...
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