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 ...
Low compliance by the country’s 8,500 small and medium enterprises (MSMEs) manufacturing pharmaceuticals would raise the risk ...
Multiple departments, including engineering and quality assurance, are responsible for evaluating GMP equipment and ...
As discussed in the Product Perspective, the Modernization of Cosmetics Regulation Act of 2022 (MoCRA) represents a major shift in cosmetic industry regulations. This article is one of a series of ...
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 ...
As the year draws to a close, medium and small drugmakers in India have a deadline coming up in less than two months as the country moves to secure the production of safe and quality medicines. After ...
New GMP compliant facility in Stuart, Florida will strengthen H2Ocean's innovation, sustainability, and in-house ...
Subject to TSX Venture Exchange (“ TSXV ”) approval, NurExone has engaged Russo Partners LLC, a New York–based strategic communications firm, (“ Russo ”) for an initial consulting project for up to ...
FDA recently published its “Good Manufacturing Practice Considerations for Responding to COVID-19 Infection in Employees in Drug and Biological Products Manufacturing Guidance for Industry” (“Guidance ...
MIAMI--(BUSINESS WIRE)--OrganaBio, LLC (“OrganaBio”) is expanding its product portfolio with the addition of current Good Manufacturing Practices (cGMP)- and current Good Tissue Practices ...
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