Revathi S has a background in pharmacovigilance and drug safety, with experience as a Drug Safety Associate at Bioclinica and Qinecsa Solutions, where case types included spontaneous, solicited, and device submissions, along with literature reviews for database validation. Currently, Revathi S serves as a Pharmacovigilance Safety Analyst at Accenture, focusing on the processing of ICSRs from various sources while adhering to global regulatory standards. An internship at Dr. Reddy's Laboratories provided foundational knowledge in pharmaceutical formulation procedures and computerized system validation.
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