I am a graduate in dentistry and total 9 years' experience with 3 years of experience in healthcare and pharmacovigilance field. Experienced in medical evaluation of adverse event reports, including but not limited to all serious and expedited reports and all pregnancy reports. • Responsible for medical review of ICSRs for accuracy, medical relevance, and overall consistency of information captured in the safety database against all the applicable supporting documents as per the client requirement • Evaluate adverse event report for seriousness, listedness, corrects coding of the adverse event and ensures that all medically relevant information from the source documents is included and provide causality assessment. • Perform final check of the case and provide medical sign off on the case. • Work and interact extensively with relevant stakeholders to ensure high quality with regard to scientific content, organization, clarity, accuracy, format and adherence to regulatory and internal guidelines, styles and processes. • Responsible for following international pharmacovigilance regulations, company and department SOPs and department and function working practices.