This workshop provides an overview of the principles of management and reporting of adverse drug reactions (ADRs) in Europe with a particular focus on the latest regulatory changes and their application in practice.

Target audience

This workshop is created for individuals who are new to pharmacovigilance or for those who want to refresh their knowledge and to find out what are the new requirements regarding reporting of the ICSRs as from November 2017.

For the absolute beginners we recommend taking our online course “PV Essentials” before attending the workshop. The course comprises 12 web-based training modules that will provide you with a comprehensive overview of the legal requirements in pharmacovigilance. More about this course you can see in our Promo module


This is a two day workshop:
Thursday, 14. September 2017 => 9:30- 15:30
Friday, 15. September 2017 =>  9:30- 15:30


Dr. Notghi Contract Research GmbH, 5. OG

Beuthstraße 7, 10117 Berlin

Click here for more information about the workshop.

We look forward to your call or your message.