Experienced and dedicated Pharmacovigilance professional with nearly 1.9 years of experience. Proven expertise in maintaining high standards of quality and productivity. Proficient in event coding and suspect product coding within the Argus Safety Database (version 8.2.3) for Individual Case Safety Reports (ICSRs). Well-versed in pharmacovigilance regulations, ensuring strict adherence to reporting requirements and safety monitoring procedures. Strong analytical skills with a keen ability to assess complex data, identify trends, and make informed decisions to enhance drug safety and patient care. Known for exceptional attention to detail and accuracy in documentation, ensuring the timely identification of safety concerns.Key strength included MedDRA coding, Case processing quality, Seriousness and Causality assessment.