PharmOut, a professional consultancy specializing in GMP compliance, has created an online database of GMP guidelines. This database, available at http://gmp.pharmout ...

An overview of the validation and qualification requirements introduced in the 2022 EU GMP Annex 1 revision, with a focus on ...

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 ...

GMP release and stability testing are indispensable elements of the pharmaceutical sector’s quality assurance strategy. These testing protocols not only ensure that pharmaceutical products are safe ...

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 Pharmaceutical Inspection Co-operation Scheme (PIC/S) has adopted new guidelines on cross-contamination in shared facilities and implemented revisions to several of the sections in its good ...

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 ...

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 ...

The Gujarat Food and Drug Control Administration (FDCA) is planning to conduct surprise inspections on units which are non-compliant out of around 4000 schedule M units in the state based on the good ...