Pharmacovigilance III

Pharmaceutical companies are required to collect and enter all adverse drug reactions reports in data bases and to report them to the competent authorities. A significant part of these adverse drug reactions must be evaluated before. The core of this workshop lies in single case evaluation. Through many practical examples and exercises you will learn step by step to write a competent evaluation.

Target audience

This workshop is aimed at everyone who needs to work with single case evaluations.


Please contact us to find out out when is the first available workshop date.

Our experts will gladly advice you personally. We look forward to your call or your message.

Click here for more information Pharmacovigilance III