Drug Lifecycle Safety Management and Pharmacovigilance Compliance

This course outlines the medical and regulatory aspects of Pharmacovigilance systems. Post-marketing support functions of a regulatory affairs department (including adverse events reporting, literature reviews, post-marketing surveillance, and summary of product characteristics, label changes, advertising, patient information and safety reporting) are examined. The principles of marketing (advertising, sales promotion and distribution) to the medical community are covered.

This course is intended primarily for students wishing to pursue a career in the pharmaceutical industry, in Clinical Research, Drug Safety, and Pharmacovigilance.

In Class Registration CAD$780 +HST        |          Online Education Registration CAD$650 +HST

in-class-reg-button                                        dist-edu-reg-button