Kavita Bhagwat PhD

Senior Regulatory Affairs Consultant

Regulis Staff Member

Kavita has over 20 years of experience in global Regulatory Affairs (EU, US, Japan, Asia, Africa, Middle-East, Latin America) across a wide range of product types including synthetic pharmaceuticals, biologicals, vaccines, recombinant DNA products, monoclonal antibodies, cosmetics, herbal medicines, medical devices and drug-device combinations. She has formulated and executed regulatory strategies for a range of small, medium and large pharmaceutical companies, guiding them through the regulatory registration maze in multiple regions and countries.


Kavita was Head/General Manager of Clinical Research and Regulatory Affairs at Nicholas Piramal India, before working in a number of consultancy roles in the UK including for Quadramed where she supported clients with regulatory strategies and drug development programmes, assessment and evaluation of dossiers, CTAs, MAAs and Quality, Nonclinical and Clinical overview writing. She did her PhD at the University of Delhi and was previously a lecturer in Pharmaceutical Chemistry.

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