Complex APIs
We offer cGMP synthesis and purification of bio-organic intermediates, excipients and bulk actives. With more than 30 years of experience and expertise in custom APIs scale-up and manufacturing for both pharmaceutical and biologics, we can effectively support your needs for:
- Polyamino acids including Poly-L-Lysine and others
- Carbohydrates
- Lipids
- Detergents
- Buffers
- Custom processes derived from a variety of plant derived natural or synthetic sources
Our Capabilities Include:
- cGMP compliant, multifaceted facility with fully validated equipment and Part 11 compliant distributive control system
- Delta V monitoring of reactos parameters, facility utilities and USP water system
- Large scale tangential flow filtrations (TFF) expertise and capability
- 20L and 200L lyophilizers
Offering you a world of capabilities
The global footprint of our API contract manufacturing services assures you of wide-ranging regulatory and supply expertise, easily accessed through a single trusted partner.
Our API Contract Manufacturing Facility Locations
- Buchs, Switzerland (cGMP)
- Madison, Wisconsin (cGMP)
- St. Louis, Missouri (cGMP)
- Schaffhausen, Switzerland (cGMP)
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