ChemCon is a contract development and manufacturing organization (CDMO) specialized in transferring drug-substance projects from R&D into fully cGMP-compliant manufacturing processes. Customers worldwide use our services to source APIs for clinical trials and/or commercial applications (i.e., orphan diseases, oncology, or emergency care), excipients, provocation substances, dietary trace elements, diagnostics, delivery agents, or reference standards. Our FDA-inspected facilities are optimized for the production of small to medium quantities.
With multidisciplinary expertise we can meet your individual demands for small-molecule organic APIs, inorganic compounds, polymers, and highly potent or controlled substances – all in full cGMP quality up to injection grade. Comprehensive in-house analytics, stability studies, documentation, and regulatory support complete our services. ChemCon looks back on an outstanding inspection history both by the FDA and European health authorities.
ChemCon is a CDMO producing solely on demand. A flexible and transparent business model allows us to accustom proposal, project course, and the final product exactly to your needs.
Our specialty is the transfer from R&D, via process validation and scale up, to fully cGMP-compliant manufacturing (injectable, ophthalmic, oral, topic grade). We take on projects at any stage of development and are set up to serve you all the way to commercial API manufacturing, including full documentation and regulatory support. Multidisciplinary competences of our experienced chemists include cGMP-compliant organic, inorganic, and polymer chemistry and the handling of highly potent and controlled substances.
Our facilities are optimized for quantities between grams and hundreds of kilograms per year. This might be of particular relevance if you wish to source specialty compounds/ excipients/ APIs that are otherwise difficult to get hold of in the desired quality and quantity.
ChemCon's cGMP manufacturing services in small to medium quantities
ChemCon GmbH, based in Freiburg, Germany, celebrates its 20th anniversary in 2017. On January 29 in 1997, Dr. Raphael Vogler (CEO) and Dr. Peter Gockel (CSO) signed the contract to found ChemCon. Today they count over 90 members of staff, and ChemCon supplies customers of the pharmaceutical industry, biotechnology companies, and research institutes worldwide.
ChemCon’s success lays in the focus on custom-made production services for APIs in the niche markets small batches, challenging process development or handling, and high toxicity. Top quality as well as occupational and environmental health and safety enjoy highest priority. Continuous investments into infrastructure and safety are an integral part of the company’s policy. Initially started on 250 m2 (2690 sq. ft.), ChemCon today occupies 4300 m2 (46000 sq. ft.) of operational space. Currently, a new production cleanroom, additional research labs as well as further offices and meeting areas are under construction.
Phone: +49 761 55970
Fax: +49 761 5597449
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