Chiracon offers the pharmaceutical industry its long-standing knowhow in the field of API synthesis (synthesis of active pharmaceutical ingredients). Chiracon has been an independent and reliable partner to the pharmaceutical and biotech industries for more than 20 years. We use the quality management system ISO 9001 and work according to GMP guidelines (Good Manufacturing Practice). Chiracon can provide you with all services possible in the field of synthetic drug development for new or generic products and can also offer the compilation of ASMF (active substance master file) / DMF (drug master file) and CMC (chemistry manufacturing and controls) / IMPD (investigational medicinal product dossier) documentation.