RMP and PSUR in life-cycle management: An art, not a miracle - Insights into RMP and PSUR preparation, assessment and regulatory management

This seminar provides insights into RMP and PSUR preparation, assessment and regulatory management.

After completing the seminar, you will:
- be able to handle your RMP updates
correctly;
- be familiar with the tasks and duties of
a QPPV in the lifecycle of PSURs and
RMPs;
- know the tips and tricks for strategic
planning and project coordination as a
pharmacovigilance writer;
- be able to handle EU assessment
reports; and
- have a good understanding of the planning, preparation and management of
additional risk-minimisation measures.

Insights into the global management of
pharmacovigilance documents round off
this seminar.