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1. In house strong validation & R&D Team.
2. The Analytical R & D (ARD) caters to API, Formulations development for generics.
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3. The ARD has ability to support small molecules, non-biological complex drugs.
4. A wide range of chromatographic separation techniques and detection techniques to meet the requirement of different types of compounds.
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5. Good residual solvents testing tools.
6. Control and monitoring of genotoxic and elemental impurities.
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7. Enantiomeric separation by normal phase HPLC & GC.
8. Stability-indicating assay and/or related substances methods for drug substances and drug products.
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9. Method development, qualification, validation and transfer.
10. Stability protocol development and program management.
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11. Stability storage, testing and data trending.
12. Cleaning validation, Detoxification studies & process validation.
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13. Pre-formulation studies, Physico-Chemical Characterization and Reverse Engineering/p>
14. In-vitro correlation studies with RLD
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15. In active collaboration for DCGI approved institutes for active bio-analytical studies to support preclinical and clinical studies during development phases.