Graduate Diploma - Clinical Research, Pharmacovigilance, and Regulatory Affairs (CRPRA)

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 students with knowledge and insight into the most recent developments in the clinical research, pharmacovigilance and regulatory affairs field.

Students 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, one will benefit from an applied and practical approach to training and develop a network of industry contacts ahead of graduation.