New Pharmacovigilance regulations for the European Union were implemented in July 2012. In this excerpt from our full webinar “Adjusting Effectively to Meeting New European Union Pharmacovigilance Requirements,” Michelle Bulliard will provide a summary of the major changes to Safety Reporting (PASS) as a result of the new regulations.

To learn more about how Quintiles can help you adjust to the new EU Pharmacovigilance requirements, email us at clinical@quintiles.com or watch the full webinar.