Adverse Events and Product Quality Complaints: A Guide for Employees

The purpose of this course is to provide an introduction to pharmacovigilance and why it is required to monitor the detection, assessment and prevention of adverse events, adverse reactions and side effects of medicinal products post marketing.

This course will cover:

• Definitions of what constitutes an adverse event and a product quality complaint
• Our obligations and what must be reported when receiving information about either of these
• A selection of examples, followed by scenarios to help you understand how to determine what is an adverse event, a product quality complaint or both

Pricing: £40

Duration: 30 minutes