From the 80 approved peptide API in new chemical entities (NCEs) and generics that are globally available, Bachem commercialized one third of these API.
Our Good Manufacturing Practice (GMP) facilities are located in Switzerland and the United States and are regularly inspected by Swiss medic, the FDA, EMA, and other local regulatory authorities in the world to ensure our operational excellence and quality.
Bachem strives to develop long-term partnerships with customers. The long-lasting experience and capability of manufacture drug substance in large quantities under GMP conditions as well as the strong regulatory background makes Bachem a preferred commercial partner.
With more than 50 years of experience in the development, production, and compiling data for Drug Master Files (DMF), we have built a reputation as a reliable GMP manufacturer of NCEs as well as for high-demand generic products.
We have the capacity to produce peptide API from gram scale up to annual quantities of hundreds of kilograms. Bachem’s quality management system covers the entire production process, from starting materials to production, packaging and delivery of the final product.
Our partners trust in our support and guidance for the commercial supply of GMP-manufactured NCEs as well as the constant quality of our generic API to manufacture their drug products.
Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.
For more information, visit www.bachem.com
To contact us, visit www.bachem.com/contact