Sanjana Reddy, M.S.

Consultant I, Regulatory Affairs

Sanjana has a Master’s degree in Regulatory Affairs and Quality Assurance from Temple University and a Bachelor’s degree in Cell and Molecular Biology from the State University of New York at New Paltzs. Sanjana has worked as a Clinical Research Coordinator at the University of Pennsylvania Surgery department where she was involved with preparation all regulatory documentation in Phase II/III clinical trials for investigational drug and device products. sAt Syner-G, Sanjana is responsible for authoring post approval submissions and providing CMC regulatory support for Syner-G clients for investigational and marketed products.

Our Focus:

At Syner-G Pharma Consulting, Chemistry, Manufacturing and Controls (CMC) is our sole focus. We offer a complete suite of CMC solutions (CMC-360) in the following three core areas: Regulatory Affairs, Pharmaceutical Development, and QA/cGMP Compliance.

Contact Us:

Syner-G Pharma Consulting, LLC
371 Turnpike Road
2 Park Central Drive, Suite #110
Southborough, MA 01772
(508) 460-9700

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