Play a critical role in development of new drugs or devices
The health industry needs trained specialists to ensure new products comply with national and international regulations. In just one year, you'll learn how to inspect and audit food and agricultural products, drugs, veterinary products, surgical equipment, medical devices and more. When you graduate, you'll be prepared to help companies gain approval to manufacture and market products.

Become a well-rounded Regulatory Affairs expert
Expand your horizons by developing an understanding of all the different aspects of Regulatory Affairs. You'll build on your previous education by broadening your knowledge in law, ethics, public health, data science and systems thinking. You'll also develop your communication, critical and analytical thinking, negotiation, project management, strategic development and collaborative skills.

Work virtually and in the real world
Learn in a collaborative and interactive environment from the comfort of your own home. Lectures are delivered remotely in simulated lecture halls, supported by case studies, research and reflective activities in our virtual reality labs. You'll then complete your program with a 360-hour paid co-op in your final semester, arming you with valuable real-world experience before you graduate.

Your postgraduate certificate in Regulatory Affairs could lead to employment with health companies; hospital and research institutes; provincial or federal government agencies and departments; contract research organizations; or research and development consulting firms.

Potential roles include:

Regulatory Affairs Specialist
Regulatory Affairs Manager
Global Regulatory Affairs Director
Quality Control and Assurance Associate
Chemistry, Manufacturing and Controls (CMC) Coordinator
Compliance Officer
Risk Management Analyst
Common Technical Documents (CTD) Specialist