 Entering serious and non-serious initial and follow-up information for ICSR Case report into the global patient safety database. Raise and manage safety queries and address in real time. Create and review comprehensive medical case narrative for expedited reports.  Retrieve and create global source cases as per client regulations and requirements. Identification of duplicate reports. Analyze the adverse event and code it with the correct medical term using MedDRA dictionary and provide causality assessment for the cases.