The first course in the 2025/2026 Regulatory Affairs in the Life Sciences Micro-Certificate series builds a solid foundation in global regulatory systems and their impact on health products.
The ATM recently concluded Introduction to Regulatory Affairs, the first course in our 2025/2026 Regulatory Affairs in the Life Sciences Micro-Certificate series. Since September, learners have been building a strong foundation in how health products navigate regulatory systems both in Canada and internationally, gaining essential knowledge for careers in life sciences and medical device regulation.
The course culminated in a hands-on workshop led by industry leader Dr. Hasnaa Fatehi, a certified MedTech regulatory affairs and quality assurance professional with over 15 years of experience across Asia, Europe, and North America. Dr. Fatehi guided participants through the assessment of medical devices before market entry, explored different regulatory pathways, and facilitated interactive exercises using real-world scenarios.
This workshop gave learners the opportunity to apply course concepts in practice, seeing firsthand how regulatory strategy is implemented in the life sciences industry. Participants left with practical insights and a deeper understanding of the regulatory landscape—knowledge they can immediately bring to professional roles or further study.
The ATM’s micro-certificate program continues to provide hands-on, applied learning for professionals and students looking to advance their expertise in regulatory affairs within the life sciences sector.