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Sreelatha Sunkari is a seasoned professional in Regulatory Affairs, currently serving as a Senior Regulatory Affairs Associate at Navitas Life Sciences since July 2018, where responsibilities include dossier compilation in ACTD/CTD format and query response preparation. Prior experience includes roles as a Regulatory Affairs Executive at TIL Healthcare, focusing on dossier compilation and query responses, and a Regulatory Officer at Madras Pharma, specializing in ROW market dossiers. Sreelatha's career began as an Executive in Quality Assurance at Actimus Biosciences Private Limited, where clinical QA auditing was performed. Educational qualifications include a Master’s in Pharmacy and a Bachelor’s in Pharmacy from Andhra University.