Quality and reliability are essential in pharmaceutical manufacturing. To ensure compliance and high standards are consistently met, the Installation Qualification (IQ), Operational Qualification (OQ) ...
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 ...
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 ...
New standards may overlook critical qualification needs. This article compares the pertinent aspects of the US Food and Drug Administration's 2009 draft guidance for industry on process validation (1) ...
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 ...
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 ...
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 ...
Dublin, June 29, 2021 (GLOBE NEWSWIRE) -- The "6-Hour Virtual Seminar on Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Systems for Regulated Industries (Pharma, Biotech, ...
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 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback