Overview
Participants will be provided with preparatory material to facilitate their learning process at the group exercises onsite.
Participants are required to bring their laptops with them for this course.
This course is aimed at the practical aspects of the 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 associated with the daily RMP job. It will provide a detailed understanding of the GVP Module V 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.
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