We help you with our cleanroom high-tech expertise

-Planning / implementation of pharmaceutical clean rooms according to EU-GMP / ISO14644 / cGMP / VDI-2083

-GMP-compliant characterization of biopharmaceuticals, vaccines and further drog- production-processes such as: solids , Semi-solids, Liquids, Sterile dosage forms and Soft gelatin capsules

-Concept and project plan for the manufacture of advanced therapy medicinal products (ATMPs) (accordance with EU GMP Part IV)

-Planning and implementation of ventilation systems in accordance with ISO 16444, ASHRAE

-Greenfield project management of GMP-Projects