Dublin, Sept. 02, 2024 (GLOBE NEWSWIRE) -- The "Master Validation Plan - The Unwritten Requirements" report has been added to ResearchAndMarkets.com's offering. As regulatory scrutiny intensifies and ...

For more than 15 years, Aldo Vidinha has worked at the intersection of engineering, quality, and regulatory strategy in the ...

Qualification/validation can be defined as “establishing documented evidence which provides a high degree of assurance that specific equipment procured will ...

To qualify and validate a pharmaceutical manufacturing facility, one must carefully review the facility design for compliance with good manufacturing practices and manage project scope definition, ...

Tivic Health® Systems, Inc. (Nasdaq: TIVC), a diversified therapeutics company, announced today it has entered a definitive agreement with Scorpius BioManufacturing to complete the GMP manufacturing ...

Title 21 CFR Part 58 provides guidance on Good Laboratory Practice (GLP) for executing non-clinical laboratory studies that support applications for research permits for Food and Drug Administration ...

Because of the growing popularity of single-use materials, the identification, characterization, and qualification of new materials used for disposable processes have become increasingly important for ...