Consistent advancement and sustainability
Our production facilities for pharmaceutical packaging components accord with a specified technological standard. Across a total production area of 1,800 m2, we work with ultra-modern injection moulding tools and fully automated assembly machines in cleanrooms with the GMP classification C/D, certified acc. ISO 14644 1-3.
We place particular value on consistent quality management acc. DIN ISO 9001. When coupled with complex technical prerequisites, we can thus avoid the generation of emissions and save valuable resources in the production of pharmaceutical synthetic components such as SFC ports, SFC caps or MFC caps.