Good Manufacturing Practice (GMP)

Good Manufacturing Practice (GMP)

Good Manufacturing Practice shall mean the practice that guarantees that medicinal products and the active substance are manufactured and controlled adequately to their intended use and in accordance with the requirements included in their specifications and documents supporting the marketing authorisation for the medicinal product.

In order to maintain the high standard of services and extend its scope, BLIRT S.A., Analytical Department has applied to the Main Pharmaceutical Inspectorate for granting the necessary authorization for control of medicinal products and investigational medicinal products.

On the November 6th 2015, Analytical Department received the authorization of Manufacture of Medicinal Products, issued by the Main Pharmaceutical Inspectorate.