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Quality Assurance
cGMP PHASE I AND PHASE II CLINICAL TRIAL MATERIAL:
Flawless clinical supply manufacturing means getting to market faster.
Analytical Services
  • Preformulation
    • Excipient Compatibility Studies
    • Differential Scanning Calorimetry (DSC)
    • Forced-Degradation Studies
    • Solubility Determination
    • Bulk Powder Characterization
  • Method Development and Validation
    • Assay
    • Related Substances
    • Chiral Purity
    • Dissolution (Apparatus I & II)
    • Cleaning Verification
  • ICH Stability Storage and Testing
    • 40˚C/75% RH
    • 30˚C/65% RH
    • 25˚C/60% RH
    • 5˚C
    • Flexible Conditions


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