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Sasi Mudumba

Sr. Director, IVD & Clinical Regulatory at Genalyte

Sasi Mudumba has worked in the field of IVD and Assay Development since 2000. In 2000, they began as a Senior Scientist at NoAb BioDiscoveries Inc, where they managed research and development, designed and evaluated immobilization of various proteins and small molecules, and developed and commercialized a successful line of products. In 2006, Sasi Mudumba moved to SQI Diagnostics Inc, where they served as Director of Assay Development and Regulatory Affairs. In this role, they managed Research and Development, Commercial Assay Validation, Regulatory Approvals, and release to Market of a regulatory approved product. Sasi achieved regulatory approvals for autoimmune diagnostic products from FDA (510k), EU (CE), and Health Canada. In 2015, Sasi Mudumba joined Genalyte, Inc. as Sr. Director of IVD, and later moved up to the role of VP of Assay Development.

Sasi Mudumba's education history consists of three degrees. Sasi obtained a PhD in Biotechnology from Jawaharlal Nehru Technological University between 1990 and 1996. Sasi then obtained an MSc in Life Sciences from the University of Hyderabad between 1985 and 1987. Lastly, they obtained a B.sc. in Microbiology from Osmania University between 1982 and 1985.

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Previous companies

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Timeline

  • Sr. Director, IVD & Clinical Regulatory

    March 1, 2023 - present

  • Senior Director, IVD

    December, 2021

  • VP, Assay Development

    November, 2015

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