Experts have recommended ICH Q10 PQS (International Council for Harmonisation - Pharmaceutical Quality System) guidelines on pharma quality systems for effective implementation of revised Schedule M ...

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 Dutch authority carrying out GMP inspections, the Health and Youth Care Inspectorate (IGJ), announced it will carry out a series of ...

Good Manufacturing Practice (GMP) is a system or protocol for ensuring product safety and consistency according to quality standards. GMP is important in all manufacturing industries, though it is ...

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 ...

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

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 ...

The FDA has issued new guidelines that exempt Phase I drugs from certain Good Manufacturing Practice regulations. In issuing the exemptions--which go into effect September 15, the agency notes that ...

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 ...

Proactive maintenance using digital tools and AI enhances GMP compliance, operational efficiency, and regulatory credibility. Facility design should integrate risk mitigation strategies, focusing on ...