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Venkata Mukkapati
Senior Regulatory Consultant

Venkata is a highly experienced Senior Regulatory Consultant with over 20 years of expertise in the pharmaceutical and allied industries. His extensive background spans Regulatory Affairs CMC, Labelling, Quality Assurance, and Production, with a robust track record in global regulatory affairs across the EU, US, and Rest of the World (RoW) markets.

Venkata possesses expert knowledge in new licensing application submissions, guiding products from Clinical Phase I through Phase III. He has held both management and consulting positions in renowned organizations, including Aurobindo, SUN Pharma, Parexel, Novartis, GSK, Eisai, and Rosemont Pharma.

Throughout his career, Venkata has demonstrated extensive knowledge in the life cycle management of established product portfolios, successfully managing numerous complex regulatory projects. His vast experience and insights have made him a trusted expert in the field, consistently delivering excellence in regulatory affairs.

Venkata is a highly experienced Senior Regulatory Consultant with over 20 years of expertise in the pharmaceutical and allied industries. His extensive background spans Regulatory Affairs CMC, Labelling, Quality Assurance, and Production, with a robust track record in global regulatory affairs across the EU, US, and Rest of the World (RoW) markets.