Reliable Services. Creative Solutions. Transparent Processes.
- From DNA to drug product in one seamless, integrated process.
- More than 35 years of experience in biopharmaceutical contract manufacturing for various molecule classes in mammalian and microbial host systems.
- Small as well as large-scale cGMP production in multi-product facilities that are approved by the major authorities (e.g. the Food and Drug Administration (FDA) in the United States, the European Medicines Agency (EMA) in Europe, and the Ministry of Health, Labour and Welfare (MHLW) in Japan).
- The confidence that you are working with a contract manufacturer that has helped bring 27 commercial biopharmaceuticals to the market – and an outstanding track record of >150 projects successfully optimized and transferred.
- Transparent processes and first-class project management – allowing you to step in at any stage of development.
- Our excellence in process science and technology helps you get your product to market faster.
- We enjoy an excellent track record with regulatory agencies, helping us to ensure smooth registration proceedings for our clients.
- More than 2,700 experienced and dedicated biopharma employees can support the successful development of your product.