(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 ...
He specializes in quality assurance, regulatory affairs, QMS / CGMP audits and problem remediation and FDA responses, new / changed product 510 (k)s, process / product / equipment including QMS and ...
Discusses HOPE-3 Phase III Trial Results and Regulatory Path for Duchenne Muscular Dystrophy Therapy December 17, ...
Discusses Progress in Blood-Purification Programs and DrugSorb-ATR's Regulatory Path December 15, 2025 11:00 AM ...
UK UK hosted a roundtable on “Where Are the Women in the UK Semiconductor Sector? Pathways for Careers in Semiconductors.” Read the full insight.
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 ...
After The Hunt' production designer Stefano Baisi on creating layers of history to match the apartment of an academic elite.
With the release of Ferrari, a major new book charting the history of the world's best-known supercar brand, we look at 10 moments that define the company's design legacy. Published by Taschen and ...
Cloud-based system quickly pulls relevant design details from past projects, speeding preparation of design drawings and ...
All In Solutions Wellness Center, a Joint Commission-accredited addiction treatment facility, highlights the essential role ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback