With 9 years of dedicated experience in the field of pharmacovigilance, I am passionate about ensuring drug safety and enhancing patient outcomes. As a Subject Matter Expert (SME), I have a strong background in Individual Case Safety Reports (ICSR), literature monitoring, and handling comprehensive safety reports including PSURs, PADERs, signal detection reports, and risk management plans.In addition to my core expertise, I bring value through my skills in Pharmacovigilance System Master File (PSMF) management, as well as the preparation and revision of Standard Operating Procedures (SOPs). My commitment to accuracy and regulatory compliance has been integral to driving safety initiatives in collaboration with global teams.I'm continuously motivated by the evolving nature of drug safety and aim to contribute to impactful, patient-centered safety measures.