Pharmacovigilance III WORKSHOP
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.
Date
29.01.2015, Berlin
26.02.2015, Berlin
11.06.2015, Berlin
20.08.2015, Berlin
08.10.2015, Berlin
05.11.2015, Berlin
10.12.2015, Berlin
Our experts will gladly provide you with personal consultation. We look forward to hearing from you soon! Contact
Click here for more information Pharmacovigilance III [498 KB]
Workshop schedule 2016