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Overview

This short course will provide a forum to discuss the experience gained with the launch of the new EudraVigilance system, the simplified ADR reporting and access principles as well as the application of the provisions set out in Good Pharmacovigilance Practice Module VI, for which revision 2 was published in the 3rd quarter of 2017.

The course will provide an update on the initial implementation experience, discuss practical examples, address frequently asked questions and next steps.

Who should attend?

This short course is designed for Qualified Persons Responsible for Pharmacovigilance (QPPVs) and pharmacovigilance experts including ICSR data entry and processing specialists.

 

Learning objectives

At the conclusion of this short course, attendees will be able to:
• Discuss recent updates to GVP Module VI based on practical examples
• Describe the initial implementation experience with EudraVigilance
• Understand the impact of the simplified adverse reaction reporting and access to EudraVigilance