Suneela Prodduturi Email & Phone Number | A pharmaceutical product development and regulatory professional with mutidisciplinary experience in the industry and USFDA. Diverse industry experience includes product development, regulatory review and strategy for complex products, program management, technical and regulatory due diligence for pipeline/ portfolio products, business development and acquisitions, gap assessments for expedited approvals and approvability assessment. Experience at FDA includes CMC review of complex drug products, management of pre-ANDA program, conducting research for complex drug products including transdermals and nanotechnology based drug delivery systems, coordination of research, review, and policy for complex products, conducting risk/gap analysis for newly approved complex NDAs to identify knowledge and research gaps and to enable expedited approval of complex products .

Suneela Prodduturi

A pharmaceutical product development and regulatory professional with mutidisciplinary experience in...
Belle Mead, New Jersey, United States

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Suneela Prodduturi’s Location Belle Mead, New Jersey, United States

Suneela Prodduturi’s Current Industry Baxter International

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Director, Global Regulatory Affairs

2023-05-01 00:00:00 - Present

Director, Regulatory Affairs

2020-08-01 00:00:00 - 2023-04-01 00:00:00

Team lead (OPQ, Immediate Office) and Reviewer (Div. of Modified Release Products)

2014-06-01 00:00:00 - 2020-08-01 00:00:00

Director, Product Development

2014-01-01 00:00:00 - 2014-06-01 00:00:00

Director, Pharmaceutical Development Center

2012-02-01 00:00:00 - 2013-12-01 00:00:00

Associate Director, Product Development

2009-04-01 00:00:00 - 2012-11-01 00:00:00

Postdoctoral Research Associate

2004-07-01 00:00:00 - 2005-03-01 00:00:00

Teaching Assistant, Analytical Chemistry

2000-01-01 00:00:00 - 2000-07-01 00:00:00

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Suneela Prodduturi is a A pharmaceutical product development and regulatory professional with mutidisciplinary experience in the industry and USFDA. Diverse industry experience includes product development, regulatory review and strategy for complex products, program management, technical and regulatory due diligence for pipeline/ portfolio products, business development and acquisitions, gap assessments for expedited approvals and approvability assessment. Experience at FDA includes CMC review of complex drug products, management of pre-ANDA program, conducting research for complex drug products including transdermals and nanotechnology based drug delivery systems, coordination of research, review, and policy for complex products, conducting risk/gap analysis for newly approved complex NDAs to identify knowledge and research gaps and to enable expedited approval of complex products .

Suneela Prodduturi has prior
experience in the following industries:
Lupin Pharmaceuticals | Fda | Pii | Steer | Aizant Drug Research Solutions Pvt Ltd Hyderabad | University Of Mississippi | University Of Louisiana At Monroe

Suneela Prodduturi has the following professional experience:
Baxter International | Lupin Pharmaceuticals | Fda | Pii | Steer | Aizant Drug Research Solutions Pvt Ltd Hyderabad | University Of Mississippi | University Of Louisiana At Monroe