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 ...

In the medical device industry, usability plays a critical role in ensuring the safety and effectiveness of highly complex medical products. The IEC 62366-1:2015 standard, which focuses on the ...

Medical device design and development is a process that helps to ensure devices that go to market are safe, effective, marketable, and profitable. The process is a blueprint of the phases needed to ...

Way back in 2001, MD+DI published an article detailing what the author considered to be The Seven Deadly Sins of Medical Device Development. The author reviewed dozens of device development programs ...

(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 ...