Parastoo Taheri

I am a pharmaceutical professional with over seven years of experience spanning Regulatory Affairs, Quality Assurance, Formulation Development, and Pharmacoeconomic. My career began in Iran’s pharmaceutical industry, where I worked with leading companies on the development, optimization, and registration of chemical drugs, supplements, and herbal medicines. I have contributed to a wide range of projects, including sustained- and modified-release anti-diabetic formulations and targeted products for pregnancy, pediatrics, menopause, and immune support.

In recent years, my focus has expanded to regulatory strategy and global market access, including the preparation of regulatory dossiers and pharmacoeconomic evaluations to support formulary inclusion and reimbursement decisions. My expertise includes GMP compliance, stability and release studies, clinical and safety data review, and close collaboration with R&D teams, manufacturers, and health authorities.

Since relocating to Canada, I have broadened my professional scope in two key directions. Alongside working as a Pharmacy Assistant in a community-pharmacy setting—where I gained hands-on experience with patient care, medication workflows, and the Canadian healthcare system—I have also been actively involved in content creation and AI-driven data analysis. I create structured, educational, and scientific content in health, pharmaceuticals, and technology, and I work with data analysis tools and AI-based methods to extract insights, support decision-making, and improve the clarity and impact of complex information.

I combine a strong scientific foundation with analytical thinking, creativity, and attention to detail. I thrive in multidisciplinary environments that value accuracy, innovation, and clear communication, and my long-term goal is to contribute to evidence-based drug development, regulatory innovation, and data-informed healthcare solutions within Canada’s pharmaceutical ecosystem.