9. Method development, qualification, validation and transfer.
10. Stability protocol development and program management.
11. Stability storage, testing and data trending.
12. Cleaning validation, Detoxification studies & process validation.
13. Pre-formulation studies, Physico-Chemical Characterization and Reverse Engineering/p>
14. In-vitro correlation studies with RLD
15. In active collaboration for DCGI approved institutes for active bio-analytical studies to support
preclinical and clinical studies during development phases.