Good Manufacturing Practice and clean room facilities

Good Manufacturing Practice

Order filling for clinical trials under clean room conditions

Good Manufacturing Practice and order filling under clean room conditions

In order to be able produce the adjuvant in sufficient quantities as well as to meet the requirements for the production of drugs a clean room plant (class A – C) was installed at ASA.

These facilities offer the opportunity of producing and filling of adjuvant or vaccine solutions under GMP conditions for your first clinical trials.

The capacity of the filling plant is around 2.000 vials per week. Therefore it is also usable for the filling of other pharmaceutical products for toxicological studies and clinical trials phase I and II.


Product data sheet: Pharmaceuticals/ GMP