ChemCon has unrivalled chemical expertise. We already worked for 25 of the largest chemical, pharmaceutical and biotech companies, 150 customers from small/midsize Biotech and Pharma, 25 customers from Research institutions and Universities and more than 10 international trading companies.
Small Molecules are our business and we are experts in what we are doing. You can rely on ChemCon´s expertise, be your product organic, inorganic or bio-inorganic.
We experienced about 100 different inspections/audits in our history: 3x by the US FDA, 4x by German / European health authorities, 15x by health, safety and environmental agencies and more than 80x by our customers or their consultants. We have never received a critical observation in company history.
ChemCon offers an unrivalled range of flexible custom chemistry services. We can always start your projects at short notice. All of us understand that ChemCon´s contribution to your project needs to fit into your plans and thus aim and schedule can change at any time.
ChemCon delivers top class communication. No matter the complexity of the synthesis we are committed to keeping you informed. You will receive clear and accurate project updates on a weekly basis. Be it a regular Telcon or direct communication with the chemist responsible for your project, Team ChemCon is always available for your queries.
ChemCon's people are key to our success. Our highly experienced, enthusiastic, and motivated team of scientists is committed to delivering your products on time, on budget and in top quality. Over 90% of our chemists are qualified to PhD level and have acquired considerable experience in all areas of small molecule synthesis.
ChemCon meets or exceeds all legislative requirements for health, safety and waste disposal. Our vast experience with highly active pharmaceutical ingredients assures that even the most active chemical compounds will be handled safely.
ChemCon is a privately owned independent company and not affiliated with any pharmaceutical company in any way. Any intellectual property generated by us during a project is the property of the customer.
ChemCon scientists and technicians are trained to deliver precise documentation, both for GMP production as well as for research. This is a vital precondition for high reproducibility and rapid approval by the authorities.
ChemCon delivers a comprehensive development record including a complete cGMP documentation set: ASMFs, DMFs (Type II), master documents, e.g. batch records, cleaning records, validation documentation, release protocols, labeling records, Certificates of Analysis and Certificates of Conformity; all in full compliance with applicable FDA guidelines.
