Pharmaceutical / Regulatory Affairs Certificates (Online)

Program Overview

AAPS’ Regulatory Affairs online courses examines the skills, techniques, and concepts required for a career in regulatory affairs. Students will become familiar with regulatory systems, legislation, and practices which relate to development, quality and manufacture of pharmaceutical goods.

Students will gain knowledge on a wide range of regulations and standards including regulatory submissions, post-approval activities, regulatory compliance, the Canadian Food and Drugs Act and Global Regulatory Strategies.


Successful candidates will also receive an online certificate per completed module:

Quality Assurance
  • Good Manufacturing Practices Level I
  • Good Manufacturing Practices Level II
  • Good Manufacturing Practices Level III
  • Introduction to Auditing Level I
  • Advanced Auditing Level II
  • Technical Writing and Scientific Communication
  • Introduction to Pharmaceutical Manufacturing Methods
Regulatory Affairs
  • Introduction to Regulatory Affairs
  • Regulatory Submissions and Preclinical – Drugs
  • Intellectual Property
  • Chemistry, Manufacturing and Control
  • Clinical – Drugs
  • Generics Drug
  • Post Approval Activities and Compliance
  • Natural Health Products
  • Biologics/Biotechnology Products
  • RA Medical Devices
  • Labeling and Product Summaries
  • Global Regulatory Strategies

To register, enroll into any online course or contact us via telephone at 416-502-2277 or by email at

Interested in AAPS? Contact us directly or provide your information for a call back.

Toronto Campus

885 Sheppard Avenue West Toronto, Ontario M3H 2T4, Canada

Hours of Operation

Mon-Fri 8:30am - 5:00pm Sat - by appointment only
Telephone: 416-502-2277 Toll Free: 1-855-502-2288 Email:
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