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About

A pharma professional, with about six years of total experience and proven track record of participating in various projects with real-time experience in planning, execution, application of methodologies and documentation. Involved in writing and review of various safety reports for global regulatory submissions, including DSURs, RMPs, PBRERs/PSURs, CARs, PADERs, and other clinical documents, as assigned. Possess a flexible and result oriented attitude. He did his Master's degree in Biotechnology from Pondicherry Central University Campus and has certification from Quintiles online ICH-GCP guidelines. He also has one national scientific publication to his credit.