
Prepare for opportunities in regulatory affairs with comprehensive post-graduate training from AAPS.
AAPS’ Professional Regulatory Affairs Post-Graduate Diploma Program provides students with the background and training needed to understand domestic and international regulatory statutes, laws, guidelines, and submission requirements.
Regulatory Affairs is a dynamic and essential profession that helps ensure safe and effective healthcare products are available worldwide. Professionals in this field support products throughout the lifecycle, from development and regulatory submission to post-marketing surveillance, compliance, and product updates.
Understand Domestic and International Requirements
Learn How Products Move Through Approval
Build Communication and Submission Knowledge
Prepare for Regulated Healthcare Industries
Graduate Employment Rate In the Field of Study
Graduate Satisfaction Rate


Understand Domestic and International Requirements
Learn How Products Move Through Approval
Build Communication and Submission Knowledge
Prepare for Regulated Healthcare Industries
AAPS’ Professional Regulatory Affairs program is designed to introduce students to the regulatory frameworks, processes, and documentation used by professionals in regulated healthcare industries.
Students explore topics related to Health Canada, the Food and Drug Administration, and international laws, regulations, and guidelines. The program also covers investigational and marketing applications, New Drug Application submissions, labeling, drug information, Electronic Common Technical Documents, Notices of Compliance, Good Clinical Practices, and ongoing post-marketing requirements.
In addition to regulatory knowledge, the program includes training in technical writing, negotiation, communication, and management skills that are important for regulatory affairs professionals working in industry environments.
The Professional Regulatory Affairs program includes courses such as:
Graduates of the Professional Regulatory Affairs Post-Graduate Diploma Program may pursue opportunities with pharmaceutical, biotechnology, medical device, natural health product, and related organizations.
Trained regulatory affairs professionals are needed to help organizations navigate complex regulatory submissions, compliance requirements, and approval processes for new and existing products.
AAPS graduates from this program have pursued careers in roles such as:

AAPS graduates have been hired by organizations including:






Take the next step toward a career in regulatory affairs with AAPS’ Professional Regulatory Affairs Post-Graduate Diploma Program.