The mixing area is used for the bulk manufacture of pharmaceutical products under controlled class D clean room conditions (ISO 14644 – class 8, US Federal Standard. 209 M6.5 and VDI 2083 class 6).
Constructed according to pharmaceutical specifications the temperature and humidity of the rooms is controlled. Purified water is produced in the water purification facility and can be directly supplied to the ring main.
Our spaciously designed filling facilities comply with international GMP regulations. The outstanding efficiency of these facilities together with a wide range of possible uses allows us to operate with a high degree of flexibility.
Because of this we are in a position to process all systems, carry out all types of filling using all kinds of containers with both combustible and non-combustible propellants and raw materials: