We operate out of St. Louis, Missouri and Seymour, Indiana. Both sites are certified and inspected by European and US regulatory agencies.
Our St. Louis facility was built in 2009.
Registered with the FDA as well as EU cGMP Certified by the Swedish Medical Products Agency (MPA).
This site has two core manufacturing capabilities.
- Specialty manufacturer of microencapsulated,
- High shear granulated particles.
Our Seymour facility was acquired in 2011. This site is registered with the FDA and has Manufacturing Site GMP Approval by German Authorities
This site has two core manufacturing capabilities
- Finished dosage form manufacturing of prenatal and prescription only iron supplements
- High volume, aqueous-based spray drying