概要
This hands-on virtual live training course is aimed at the practical aspects of the EU Risk Management Plan (EU RMP) creation process. We will demonstrate the various uses of the EU RMP within the lifecycle of medicinal products, medical writing process and RMP management process. It will provide a detailed understanding of the GVP Module V (Rev 2) with all potential implications for the marketing authorisation holders.
The participants will learn the best practice in medical writing of the EU RMP. The solutions will be demonstrated in practical exercises included throughout the course.
