This program focuses on developing regulatory strategies for the approval of health products. In just one year, you'll learn how to inspect and audit a variety of health-related products including food, drugs, veterinary products, and medical devices. The program prepares students to help companies gain approval to manufacture and market products by ensuring compliance with national and international regulations. Delivered fully online, the course offers a collaborative and interactive environment with real-time classes, case studies, and virtual labs. The program culminates in a 360-hour paid co-op, giving practical industry experience before graduation.
Why this course is highly recommended
Although the program is not currently accepting applications, the comprehensive curriculum prepares students for careers in regulatory affairs across health companies, government agencies, research institutes, and consulting firms. Its focus on real-world experience through a paid co-op and the development of diverse skills makes it a valuable pathway into the health products industry.
The program broadens your understanding of all aspects of Regulatory Affairs, including law, ethics, public health, data science, and systems thinking. It aims to develop well-rounded regulatory experts with skills in communication, critical thinking, negotiation, project management, and strategic development.
Application fees
10.78L
1st year tuition fees
10.78L
Living cost
Applicants need a postsecondary bachelor’s degree, an advanced diploma, or a diploma in science, health science, or a related field. Preference is given to students with a degree in a science or health science stream. A minimum overall GPA of 65% is required, and other degrees such as MA, PhD, or MD in relevant fields are also considered.

English language test
Want to learn more about the admission process, eligibility criteria,
and acceptance rates for international students? Visit the Sheridan College admission page
for complete details.
Graduates can pursue roles such as Regulatory Affairs Specialist, Manager, or Director. Other opportunities include Quality Control and Assurance, CMC Coordinator, Compliance Officer, Risk Analyst, and CTD Specialist. These positions are available in health companies, hospitals, government agencies, research organizations, and consulting firms.