Developing a cutting edge medical device can be really fun and exciting. There’s always something to test and do and learn from. You have that great feeling you’re changing the world. However, ...
Dublin, Nov. 26, 2025 (GLOBE NEWSWIRE) -- The "Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) for Medical Devices Training (Nov 13, 2025)" training has been ...
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) Dublin, Jan. 17, 2024 (GLOBE NEWSWIRE) -- The "Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) - A Technical Documentation ...
Overview: The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device ...
(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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