Good Manufacturing Practice (GMP) stands for Good Manufacturing Practice for medicinal products.
GMP ensures that patients receive medicines of uncompromisingly high quality. These quality requirements must be met during the manufacture, processing, packaging and storage of medicinal products. Facilities worldwide must follow GMP regulations in order to obtain a Manufacturing Authorization.
The aim is to bring safe, effective and harmless medicines onto the market.
All parties involved in the manufacture of medicinal products or active ingredients must comply with GMP regulations.
Here, too, we provide you with the necessary know-how and are happy to support and advise you in the context of setting up, optimizing and maintaining your GMP quality management system.