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 ...

This article explores the US and EU compliance requirements to ensure patient safety for GMP ancillary materials in cell and ...

Low compliance by the country’s 8,500 small and medium enterprises (MSMEs) manufacturing pharmaceuticals would raise the risk ...

Manufacturers are usually subjected to a diverse variety of regulations typically established by international and regional bodies. Failure to comply can result in the loss of authorization and ...

Small biotechs in early development of cell therapies are often surprised by the strictness of commercial manufacturing standards. That’s the view of Luděk Sojka, PhD, CEO of contract developer 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, ...

Small drugmakers seek deadline extension for GMP compliance as December 2025 approaches, emphasizing the need for support and ...

The health ministry is unlikely to extend the Schedule M deadline for MSME pharma firms beyond December 31, 2025, as it ...