Auditor Ph.D., is a seasoned pharmacovigilance and quality professional with 5 years of experience in the Canadian pharmaceutical industry. Her expertise includes managing pharmacovigilance activities, developing inspection readiness programs, coordinating with global partners, and handling adverse event reports and medical inquiries. She is well-versed in GMP guidelines, GVP practices, Health Canada regulations, and international standards. She has consistently received above-expectation ratings during her tenure at Natco Pharma (Canada) Inc. Anamika holds a Ph.D. in Biotechnology, a postgraduate diploma in Regulatory Affairs and Quality Assurance, and an M.Sc. in Life Science. She is a detail-oriented, self-motivated professional known for her adaptability and ability to manage multiple projects.