The "How to Interview During GMP (Good Manufacturing Practice) Audits Training Course (Mar 12, 2026)" training has been added to ResearchAndMarkets.com's offering. Ensuring compliance with Good ...
Low compliance by the country’s 8,500 small and medium enterprises (MSMEs) manufacturing pharmaceuticals would raise the risk ...
Small drugmakers seek deadline extension for GMP compliance as December 2025 approaches, emphasizing the need for support and ...
Dublin, Nov. 03, 2025 (GLOBE NEWSWIRE) -- The "Golden Rules of Being a Successful GMP (Good Manufacturing Practice) Auditor Training Course (Feb 5th - Feb 6th, 2026)" training has been added to ...
The health ministry is unlikely to extend the Schedule M deadline for MSME pharma firms beyond December 31, 2025, as it ...
Multiple departments, including engineering and quality assurance, are responsible for evaluating GMP equipment and ...
GMPs require high cleanliness and maintenance standards to prevent contamination and ensure product quality in pharmaceutical manufacturing. Risk-based maintenance programs focus on critical assets, ...
Combining cell and gene therapeutic approaches is reshaping basic and translational research, yielding new models and tools that help scientists delve deeper into the drivers of health and disease.
PORT WASHINGTON, N.Y.--(BUSINESS WIRE)--Aceto, a leading global provider of specialty materials for life sciences and advanced technology end markets, announced today its acquisition of A&C Bio Buffer ...
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