Anagha Patil

I am a reliable drug safety specialist with over four years of experience in pharmacovigilance, focused on adverse event reporting, signal detection, and regulatory compliance. I have a strong track record of optimizing end-to-end ICSR workflows and aggregate reporting.

I have led literature surveillance operations, trained and mentored junior analysts, and collaborated closely with medical, clinical, and regulatory teams to drive patient safety initiatives. My work has included case intake, triage, medical coding, narrative writing, peer review, and follow-up.

I combine scientific training (M.Pharm) with practical pharmacovigilance skills—GVP, literature search, medical writing, and data analysis—while maintaining strong communication, time management, and presentation abilities to support high-quality safety outcomes.