- Method Development and Validation
- Product Development
- Cosmetics Testing
- USP Testing
- Raw Material Testing
- Analytical Testing
- Impurity Identification
- Liquid Chromatography Analysis
- Finished pharmaceutical products
- Gas Chromatography Analysis
- Method development activities to support de-formulation studies and determination of active/excipient ratios
- Method Development Phase I, II, III
- Release Testing
- Raw material and Excipients testing
- Proof of structure
- Identification and quantitation
- Establishment of purity as well as release
- Specification development for excipient-masking transformations
- Container-closure integrity evaluations
- Extractable/leachables determinations
- Establishment of purity as well as release
- Impurity Identification
- Reverse Engineering
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- Bioanalytical Assay Development and Validation
- Stability Testing
- Protein Analysis
- Stability Indicating Assays
- Chromatographic Purity Method Development and Validation
- Dissolution Testing
- Research and Development
- Stability Indicating Assays
- Solid oral - assay, impurities, dissolution, disintegration, moisture, hardness, friability, content uniformity, and cleaning methods.
- Liquid oral - assay, impurities, dose uniformity, osmolalility, viscosity, pH, and cleaning methods.
- Topical - assays, impurities, pH, viscosity, dissolution, moisture, and microbial methods.
- Method development activities to support deformulation studies and determination of active/excipient ratios
- Excipient identification and quantitation
- Packaging components
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