Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You’ll learn about what processes needed to be ...
For laboratories that operate within a quality management system, compliance with global standards such as ISO 9001, ISO 13485, ISO 17025, ISO 15189, GxP, and other country-specific regulations ...
Dublin, June 04, 2025 (GLOBE NEWSWIRE) -- The "Master Validation Plan - The Unwritten Requirements Course" training has been added to ResearchAndMarkets.com's offering. FDA Warning Letters and recent ...
Syngene, a world-leading manufacturer of image analysis solutions, has announced that it has produced new software and validation information for its Dyversity, G:BOX and GeneGnome range of image ...
TEKLYNX label security and traceability software, plus validation accelerator pack, streamlines label approval and audit readiness for medical device manufacturer AUCH, France, May 25, 2022 ...
Syngene has announced that it has produced new software and validation information for its Dyversity, G:BOX and GeneGnome range of image analysis systems. This makes them ideal for scientists in ...
(MENAFN- GlobeNewsWire - Nasdaq) FDA Warning Letters highlight critical cGMP deficiencies in V&V planning. Discover how to optimize Master Validation Plan elements against ISO 14971 for effective ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results
Feedback