On 8 December 2017, detailed EU guidelines on good manufacturing practices (“GMP”) for investigational medicinal products for human use were adopted by the European Commission under the EU Clinical ...

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 ...

In August 2022, the European Commission published a revision to Annex 1 “Manufacture of Sterile Medicinal Products” in EudraLex - Volume 4 - Good Manufacturing Practice (GMP) guidelines that will ...

New Delhi: The government will shortly notify a revised version of good manufacturing practices (GMP), at par with the World Health Organization (WHO) standards, for small pharmaceutical companies ...

Dublin, Dec. 04, 2024 (GLOBE NEWSWIRE) -- The "GMP Auditing for Quality Assurance Training Course" training has been added to ResearchAndMarkets.com's offering. This course is recommended for ...

BEIJING, May 24, 2013 -- Sinovac Biotech Ltd. (NASDAQ: SVA), a leading provider of biopharmaceutical products in China, announced that Sinovac Beijing, the main operating subsidiary company of Sinovac ...

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 ...

Chennai: The implementation of Revised Schedule M guidelines for small and medium pharma companies by the end of this year will increase the capex requirements of the industry. This may also lead to ...

HOLLISTON, Mass.--(BUSINESS WIRE)--Oligo Factory, a leading manufacturer of high-quality oligonucleotides at scale, announces today that it is compliant with current Good Manufacturing Practices (GMP) ...