The demand has never been greater for professionals who can help companies ensure compliance with applicable laws and regulations in the development and commercialization of new drugs and healthcare products. The Clinical Research, Pharmacovigilance and Regulatory Affairs program will provide you with knowledge and insight into the most recent developments in the clinical research, pharmacovigilance and regulatory affairs field.
| Province | Ontario |
|---|---|
| Colleges | Academy Of Applied Pharmaceutical Sciences |
| Program Categories | Healthcare |
| Program Duration | 1 Year |
| Program Intakes | January, February, April, May, June, August, October, November |
| Class Type | Hybrid |
| Funding | OSAP, Government Student Loans |
The demand has never been greater for professionals who can help companies ensure compliance with applicable laws and regulations in the development and commercialization of new drugs and healthcare products. The Clinical Research, Pharmacovigilance and Regulatory Affairs program will provide you with knowledge and insight into the most recent developments in the clinical research, pharmacovigilance and regulatory affairs field.
You will learn current regulatory and pharmacovigilance research current clinical research topics including Good Clinical Practices (GCP), regulatory submission, pharmacovigilance regulations and Good Pharmacovigilance Practices (GVP), and quality assurance concepts in clinical trials and pharmacovigilance. As a student in this program, you will benefit from an applied and practical approach to training and develop a network of industry contacts ahead of graduation.
CRPRA Program Brochure
Career Opportunities
Graduates of the Clinical Research, Pharmacovigilance and Regulatory Affairs Post-Graduate Diploma Program can pursue careers in the Pharmaceutical, Biotechnological, Medical devices, Cosmetics, Natural health Products, and allied industries. Trained and qualified RA professionals are in demand for pharmaceutical, biotech, medical device and natural health product companies as they are needed to navigate the intricacies of regulatory submissions for new products.
AAPS graduates have been hired as:
Clinical Research Coordinator
Pharmacovigilance Data Management Associate
Clinical Research Associate
Pharmacovigilance Associate
Clinical Data Management Associate
Clinical Research Project Leader
Pharmacovigilance Project Leader
Clinical Research Monitor
Medical Information Associate
Pharmacovigilance Officer
Quality Assurance in Clinical Research
Quality Assurance in Pharmacovigilance
Auditor in Clinical Research and Pharmacovigilance
Quality Assurance Associate/Technician
Auditor/Inspector
Technical Writer
Document Reviewer
Regulatory Affairs Associate
Regulatory Compliance
Regulatory Operations Associate
