UPM Manufacturing Facility

UPM’s 30,000 sq foot main facility in Baltimore features a cGMP pharmaceutical manufacturing suite as well as analytical and R&D laboratoris staffed by industry veterans.
Whatever form your product takes, we ensure rigorous and technically sound product characterization, methods development, and QC release.

MAIN FACILITY

Formulation Evaluation
  • Content uniformity evaluation
  • Dissolution testing
  • Stability assessment
Regulatory Support
  • SUPAC application support
  • GMP/FDA/ICH guidance
  • Product development strategies
Analytical Services
  • HPLC based
  • Full ICH stability conditions
  • Dissolution testing
Clinical Manufacturing
  • cGMP manufacturing
  • Direct API fill into capsules
  • Dosage form preparation and blinding




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