Bachelor in Pharmaceutical Regulatory Affairs & Quality Operations

Tuition is International student tuition is $18,500 CAD for the full programme.; the deadline to apply for the Sep 2026 intake is Aug 31, 2026.

Ensuring that pharmaceutical products meet rigorous safety, efficacy, and quality standards is one of the most critical challenges in global healthcare. The Pharmaceutical Regulatory Affairs & Quality Operations (RAQ) graduate certificate at Seneca Polytechnic is designed for professionals looking to navigate the complex legal and scientific frameworks governing the drug and medical device industries. By bridging the gap between theoretical compliance and real-world application, this program prepares graduates to manage the entire lifecycle of health products, from initial development and clinical review to manufacturing and final market authorization.

Specialized Industry Focus

This intensive one-year program offers a deep dive into both Canadian and international regulatory landscapes. Students develop a technical fluency in health legislation, Good Manufacturing Practices (GMP), and the submission processes required by agencies like the Therapeutic Products Directorate. Whether you are aiming to work as a regulatory affairs associate or a quality assurance investigator, the curriculum emphasizes the practical skills needed to maintain product integrity and manage the high-stakes review processes that define modern pharmaceutical operations.

• Gain proficiency in navigating complex health care legislation and guidelines.
• Master the documentation and submission processes for therapeutic products.
• Develop a strategic understanding of manufacturing processes and their regulatory impact.
• Benefit from optional work terms that provide hands-on, industry-relevant experience.