GVP is drawn up to facilitate the performance of pharmacovigilance activities within the EU and applies to marketing authorisation holders in the EU, the Agency and competent authorities in Member States. GVP is being developed within a governance structure set up by the Agency and national competent authorities specifically for the implementation of the new pharmacovigilance legislation. This online training will explore the reasons for the existence of GVPs, Proper organisation of PSMF and key principles on audit design preparation. #webinar
Key learnings:
Existence
Existence
Role
Functions
Meaning
Risk Management
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