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Geeta Pamidimukkala has extensive work experience in the field of regulatory affairs and policy analysis in the medical industry. Geeta currently holds the position of Vice President of Technology and Regulatory Affairs at AdvaMed since 2022. Prior to that, they worked at the FDA from 2015 to 2022, where they held various roles such as Deputy Division Director and Acting Deputy Division Director, overseeing premarket programs and providing technical direction for the implementation of MDUFA IV commitments. Geeta also represented the Office of Device Evaluation (ODE) during MDUFA IV negotiations with industry and patient groups. Geeta Pamidimukkala has been with the FDA since 2008, where they initially served as the Lead Scientific Reviewer, conducting safety and efficacy evaluations of medical devices and combination products. Geeta also worked as the 510(k) Program Manager at the Center for Devices and Radiological Health, Office of Device Evaluation (ODE), where they developed regulatory policies, authored guidance documents, and managed the Refuse to Accept (RTA) program. Before joining the FDA, Geeta Pamidimukkala worked as a Bioanalytical Scientist at Roche from 2004 to 2006.

Geeta Pamidimukkala earned a Bachelor of Science (BS) degree in Electrical and Electronics Engineering from Tufts University in 2004. Geeta then pursued a Master of Science (MS) degree in Biomedical/Medical Engineering at the New Jersey Institute of Technology from 2006 to 2008. Additionally, they obtained another Bachelor of Science (BS) degree in Electrical and Electronics Engineering from Tufts University in 2004.