Market opportunities lie in enhancing risk-based V&V planning, focusing on DQ, IQ, OQ, and PQs to address cGMP deficiencies and regulatory expectations. By aligning with FDA, ICH, and ISO standards, ...

BioX生物安全柜IQ/OQ/PQ的工作原理介绍？ BioX生物安全柜IQ/OQ/PQ的使用方法？ BioX生物安全柜IQ/OQ/PQ多少钱一台？ BioX生物安全柜IQ ...

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 ...

This half day workshop addresses current regulatory requirements for qualification of analytical instruments, laboratory personnel and GMP compliance. It defines DQ/IQ/OQ and PQ and provides a hands ...

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 ...

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 This article compares the pertinent aspects of the US Food and Drug Administration's 2009 draft guidance for industry on process validation (1) ...