DUBLIN--(BUSINESS WIRE)--The "6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, Devices)" webinar has ...
The "Master Validation Plan - The Unwritten Requirements Course (November 18, 2025)" training has been added to ResearchAndMarkets.com's offering. FDA Warning Letters and recent high-profile recalls ...
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 ...
(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 ...
TESTA Analytical announce new 21CFR Part 11 compliance software for use with its popular family of NanoBrook particle sizing and zeta potential instrumentation. Determination of particle size and zeta ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results