You'll learn about current regulatory and pharmacovigilance research, including GCP, regulatory submission, pharmacovigilance legislation, and Good Pharmacovigilance Practices (GVP), as well as quality assurance ideas in clinical trials and pharmacovigilance. You will benefit from an applied and practical approach to training as a student in this programme, and you will create a network of industry contacts before graduation.

Graduates of Pharmacovigilance, and Regulatory Affairs might work in the pharmaceutical, biotechnological, medical device, cosmetics, natural health products, and allied industries. Pharmaceutical, biotech, medical device, and natural health product companies all need trained and competent RA specialists to help them negotiate the complexities of regulatory applications for new products.

Post Graduate Certificate – BSc. or higher level of education.