ChemCon

ChemCon operates as an internationally recognised contract development and manufacturing organisation (CDMO) based in Freiburg, Germany. The company specialises in the synthesis and analysis of pharmaceutical ingredients (APIs) and fine chemicals, with a strong emphasis on GMP compliance. ChemCon provides services to customers globally, aiding in the sourcing of APIs for clinical trials, registration, and commercial applications, particularly in areas such as orphan diseases, oncology, and emergency care. With a commitment to transferring R&D projects into fully cGMP-compliant manufacturing processes, ChemCon has built a strong reputation over its years of operation. The facilities, which have been inspected by FDA and German authorities 16 times, are optimally structured for the production of small to medium quantities. Their multidisciplinary expertise enables tailored solutions for small-molecule organic APIs, inorganic compounds, and polymers. Their services are further enhanced by comprehensive in-house analytics, stability studies compliant with ICH guidelines, detailed documentation, and regulatory support.

Services include:
- Analytical Services
- cGMP Synthesis
- Chemical Analysis
- Contract Manufacturing (CMO)
- Manufacturing
- Custom Synthesis
- DMF Establishment / Maintenance
- Feasibility Studies
- APIs (Active Pharmaceutical Ingredients)
- Parenterals
- Small Volume
- Process Development
- Process Validation Studies
- Stability
- ICH
- Regulatory Services
- Containment
- Contract Development and Manufacturing (CDMO)
- Small Molecule
- Drug Substance Manufacturing (API)
- Research & Development
- Clinical Trial Materials
- Analytical Methods Development

ChemCon remains dedicated to providing high-quality services tailored to meet the specific needs of its clients in the pharmaceutical industry. For more information, please visit chemcon.com.