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 ...
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 ...
DUBLIN--(BUSINESS WIRE)--The "How to Deal with Difficult Situations in GMP (Good Manufacturing Practice) Audits Training Course (March 5, 2026)" training has been added to ResearchAndMarkets.com's ...
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 ...
In the world of pharmaceuticals, companies aim to operate under GMP guidelines — a set of production and manufacturing measures to assure standards for medicinal products. But too often, the reality ...
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 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results