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.
For the pharmaceutical industry and for compounding for pharmacies and hospitals
GMP manufacturing of drugs for clinical trials, including the compilation of the related documentation (IMPD)
Selected chiral intermediates for the synthesis and industrial applications