Geetha Tula, M.S.

Consultant I, Regulatory Affairs

Geetha has a Master’s degree in Chemistry-Molecular Biochemistry from Sacred Heart University and a Bachelor’s degree from India in Pharmacy. Geetha has worked as a CMC Regulatory Specialist at Merck where she was involved in Executing regulatory Post-Approval filing strategies and variations for global products while ensuring that all regulatory documents are prepared accurately, completely and on-time. At Syner-G, Geetha 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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