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Tejasvi Pasi is a seasoned regulatory affairs professional with extensive experience in the medical device and digital health industry. Currently serving as Senior Manager of Regulatory Affairs at Glooko since December 2012, Tejasvi leads strategies and submissions for SaMD, digital therapeutics, and digital health products, with expertise in FDA 510K submissions and European CE mark requirements. Prior roles at Glooko include Regulatory Affairs Manager and Associate, where responsibilities encompassed managing regulatory and quality activities and overseeing submissions. Tejasvi's earlier experience at Nostrum Laboratories involved submitting ANDA-related documents for solid oral formulations and compiling regulatory documents in eCTD format. Academic qualifications include a Bachelor's degree in Pharmacy from Andhra University and coursework at UCSC.