Manpreet Kaur

About Manpreet Kaur

Hello and welcome to my LinkedIn profile!I am a passionate and detail-oriented Pharmacovigilance Scientist with a strong background in healthcare. My journey in this field has been shaped by my educational foundation in dentistry and a post-graduation in Hospital Administration from the prestigious Apollo Institute of Hospital Management.In my current role as a Pharmacovigilance Scientist, I play a pivotal role in safeguarding patient health by meticulously reviewing and evaluating adverse event reports. I pride myself on being a guardian of drug safety, ensuring that every report is complete, accurate, and compliant with regulatory standards.My expertise lies in: Peer Review: Confirming the completeness and consistency of cases in the safety database, aligning them with case processing guidance documents. Data Analysis: Prioritizing cases based on receipt date and seriousness, performing coding using industry-standard dictionaries, and ensuring causality is accurately captured. Documentation: Maintaining meticulous contact logs, evaluating reports for seriousness and listedness, and providing medical sign-offs. Global Compliance: Staying up-to-date with international pharmacovigilance regulations and adhering to company and department SOPs.I am genuinely passionate about healthcare and am committed to making a meaningful impact in the field. I am eager to connect with like-minded professionals, share knowledge, and explore opportunities to contribute further to the healthcare sector.If you\'re interested in discussing collaborations, industry insights, or anything related to healthcare and pharmacovigilance, please don\'t hesitate to reach out. Let\'s connect and create a safer and healthier world together!

Experience

1. Associate - Drug Safety Physician Ii

   Indegene

   Oct 2021 — Present · Bengaluru, IN

   Conduct comprehensive peer reviews to ensure the safety database\'s data integrity and adherence to case processing guidance documents. Assess source documents for essential information, such as patient identification, reporter identification, adverse events/reactions, and suspect or interacting drugs, to validate the safety report. Prioritize cases based on receipt dates and seriousness, ensuring timely attention to critical issues.Scrutinize the coding of company suspects using CDD (company drug dictionary) and co-suspect/concomitant medications with WHODD to maintain accurate records. Verify the accuracy of event coding and assess the correctness of causality attribution within each case. Confirm the alignment of reported events with reference safety information (RSI) documents, distinguishing between listed, expected, unlisted, and unexpected events. Monitor event or case updates and ensure appropriate follow-up actions are taken for completeness. Oversee discrepancies, seriousness upgrades, and split notifications through diligent action item verification. Manage case linking, encompassing E2B linked reports and cross-linked reports for comprehensive data analysis. Review and enhance narrative completeness and correctness as needed. Maintain detailed contact logs for documentation purposes. Conduct medical evaluations of adverse event reports, including serious, expedited, and pregnancy-related cases. Ensure accuracy, medical relevance, and overall consistency of information in individual case safety reports (ICSRs) by aligning them with supporting documents, as per client requirements. Assess adverse event reports for seriousness, listedness, and correct coding, incorporating all medically relevant information from source documents and providing causality assessments. Perform final case checks and provide medical approval for closure. Track inconsistencies in activities conducted by data entry and QC reviewers based on established checklists. C

Education

• Uttaranchal Dental and Medical Research Institute

  Bachelor of Dental Science

  2010 — 2015

• Apollo Institute of Hospital Administration

  Masters of Hospital Administration

  2016 — 2018