This article explores the US and EU compliance requirements to ensure patient safety for GMP ancillary materials in cell and gene therapy (CGT) manufacturing.
Concerned over incorporation of strict WHO, ICH guidelines in the proposed revision of Schedule M, the pharmaceutical industry in the country has urged the Union health ministry to revise the Schedule ...
Independent certification from global public health organization NSF demonstrates a commitment to personal care product quality and compliance with U.S. GMP requirements FARGO, N.D., June 25, 2025 ...
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 ...
EMA's work plan emphasizes supply chain integrity, product quality, and new manufacturing technologies' impact on the supply chain. Revised GMP guidelines include updates to documentation, digital ...
insights from industryDr. Irma Börcsök and Dörte Keimer CEO and Head of Quality AssurancePromoCell In this interview, News-Medical talks to Dr. Irma Börcsök (CEO of PromoCell) and Dörte Keimer (Head ...
Oligo Factory, which manufactures oligonucleotides at scale, reports that it is compliant with current Good Manufacturing Practices (GMP). This milestone emphasizes Oligo Factory’s commitment to ...
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