Chiracon GmbH has 20 years of experience in the field of drug synthesis and documentation. As a German, Berlin-Brandenburg based company the company can reliably offer all services possible in the field of synthetic drug development for new or generic products. We specialize in organic synthesis, scale up and production. Furthermore we provide all the documentation needed for active pharmaceutical ingredients (APIs) for clinical trials, and also in order to introduce new APIs to market - ASMF (active substance master files) /DMF (drug master files), Pharmaceutical Quality/CMC (Chemistry, Manufacturing and Controls) /IMPD (Investigational Medicinal Product Dossier). We utilize a management system which is based on an integrated ISO9001 system and includes a GMP environment.