Drug Safety Associate
I serve as an integral member of the Pharmacovigilance team at WiproLtd., where I handle the entry of Individual Case Safety Reports (ICSR) datainto the database. My responsibilities include crafting detailed narrativesand executing precise MedDRA coding for various adverse events. I alsomanage the merging of duplicate forms to ensure that all relevantinformation is accurately included. In addition, I conduct follow-upactivities with healthcare professionals (HCPs), non-HCPs, and othercompanies to gather additional information. I assess product complaints,identify suspect products, and file the necessary product complaints.Additionally, I oversee product refunds and replacements in specificscenarios, ensuring that all actions are compliant with regulatoryguidelines.