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 ...

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

Digital GMP expectations are increasing, driven by Annex 11 and Annex 22, necessitating robust lifecycle management, data ...

Dear reader, the pharmaceutical industry plays a crucial role in protecting human health, which necessitates stringent ...

Key market opportunities include identifying emerging trends and innovations, leveraging insights from recent mergers and acquisitions, optimizing supplier selection, staying informed about regulatory ...

Eramol’s purpose-built sterile manufacturing facility at the Sevenoaks campus is in the final stages of commissioning and ...

Multiple departments, including engineering and quality assurance, are responsible for evaluating GMP equipment and ...

Cipla had earlier received final USFDA approval in May 2024 to market its generic Lanreotide injection in multiple strengths.

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

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Ayush Quality Mark to certify companies with valid accreditations to global standards for EoDB: Dr Tripta Dixit, Ayushexcil: Shardul Nautiyal, Mumbai Wednesday, January 7, 2026, 0 ...

Ayush Quality Mark to serve as a global benchmark for authenticity & excellence: Experts: Shardul Nautiyal, Mumbai Wednesday, January 7, 2026, 08:00 Hrs [IST] Companies with valid ...