Immunology, Immuno-oncology, Pharmacology and Toxicology, Pharmaceutical formulation development, Pharmacokinetics and Nanomedicine.

Versatile knowledge and experience in interdisciplinary domains lead to accelerate the delivery of projects as per milestones of organizations and with current market dynamics.

  • Strong expertise in pre-clinical studies, pharmaceutical formulation development, Drug product process development and analytical characterization.

  • Leading expert in key impurity areas, including Mutagenic impurities (MIs), Elemental impurities (EIs), impurity qualification, different strategies on impurity characterization, Risk Assessment and comprehensive evaluation of Extractables and Leachable profile studies and their significance in Pharmaceutical Quality.

  • Competent analytical research and quality management professional, collaborative and dynamic leader with global relationship management proficiency who can build consensus and influence outcome.