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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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