Evaluation,prioritizatiozion and processing of adverse events in the global safety database within agreed timeframe and to a high standard of accuracy in compliance with standard operating procedures and global regulatory requirements.Performing duplicate check for valid cases as per client requirements, consistent data entry and processing from source documents adhering to timelines and quality.Confirm consistent coding of medical history and adverse events.Assesing ADR for labelling including USPI.
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Akshara M Pillai — Pharmacovigilance Service Associate at Accenture in Bengaluru, IN | Unifers