Chiracon GmbH

Key figures

• 20 years of experience in the field of drug synthesis and documentation
• offer all services possible in the field of synthetic drug development for new or generic products
• specialize in organic synthesis, scale up and production
• provide all the documentation needed for active pharmaceutical ingredients (API) for clinical trials, and 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)

• utilize a management system which is based on an integrated ISO9001 system and includes a GMP environment

We offer

• regulatory affairs
• API synthesis
• API for clinical trials
• API analytics