Overview
This virtual live training course covers essential concepts and guidance about the Pharmacovigilance System Master File (PSMF).
This key document describes the company’s pharmacovigilance system, supporting, and documenting its compliance with the requirements laid down in the EU legislation and is the first document requested by a Competent Authority in preparation of a pharmacovigilance inspection.
The entire course is in line with the guidelines on EU Good Pharmacovigilance Practices GVP Module II – Pharmacovigilance System Master File (rev. 2), Commission Implementing Regulation (EU) No. 520/2012, and relevant EMA guidelines.
Participants benefit from hands-on expertise on best practices shared by trainer with extensive experience regarding PSMF including the EU-QPPV perspective.
Ample time is set aside for Q&A and interactive discussions.
Participant Testimonials
A well-informed training session with good audience participation. Appreciated the MHRA providing clear guidance. – Sara Santosh Expedith – PV Risk Specialist, Novo Nordisk, United Kingdom
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