(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 ...

The "3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS" training has been added to ResearchAndMarkets.com's offering. This webinar will examine ...

Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical ...

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 ...

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 ...