Complex APIs

API Synthesis

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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Research. Development. Production.

We are a leading supplier to the global Life Science industry with solutions and services for research, biotechnology development and production, and pharmaceutical drug therapy development and production.

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