The market opportunity lies in providing specialized GMP auditing courses to pharmaceutical professionals, enhancing their skills in compliance, evaluation, and reporting, thereby ensuring ...

This article explores the US and EU compliance requirements to ensure patient safety for GMP ancillary materials in cell and gene therapy (CGT) manufacturing.

In the pharmaceutical industry, cleanrooms are categorized based on the level of airborne particle concentration necessary to meet the cleanliness standards required for the specific manufacturing ...

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 ...

Europe has long been the center of global active pharmaceutical ingredient (API) production, but producers in India and China are rapidly eroding the region's leading position. When it comes to making ...

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 ...

STOCKHOLM, SWEDEN / ACCESSWIRE / May 17, 2024 / QuTEM AB (formerly Vironova BioAnalytics AB), a leading provider of transmission electron microscopy (TEM) services, proudly announces the receipt of ...

This Auditing for GMP course is specifically designed to address the challenges of GMP auditing for the pharmaceutical industry and present the basic competencies required to effe ...