• 1. In house strong validation & R&D Team.

    2. The Analytical R & D (ARD) caters to API, Formulations development for generics.

  • 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.

  • 5. Good residual solvents testing tools.

    6. Control and monitoring of genotoxic and elemental impurities.



  • 7. Enantiomeric separation by normal phase HPLC & GC.

    8. Stability-indicating assay and/or related substances methods for drug substances and drug products.


  • 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.

    15. In active collaboration for DCGI approved institutes for active bio-analytical studies to support preclinical and clinical studies during development phases.