The Global Forum for Qualified Person for Pharmacovigilance (QPPV) covers topics such as:
- Risk Minimisation – Medication beliefs and behaviours, EU requirements
- Two years later – Impact of the new EU PV requirements on the QPPV role
- Networks and Communication – Sources of information for QPPVs
- Metrics and KPIs – Support for QPPV oversight
- Quality Systems – Compliance with GVP Module 1
- Being a QPPV in Different Environments (non- EU companies, contract QPPVs etc.)
- Operational Challenges; e.g. the PSMF, in place and meeting Regulator needs?
- PV Inspections – What’s new and what’s old (but still being found…)
The Global Forum for Qualified Person for Pharmacovigilance (QPPV) brings together:
- Deputy Qualified Persons for Pharmacovigilance
- EEA Qualified Persons for Pharmacovigilance
- CRO and Consultants providing QPPV Services
- Senior Pharmacovigilance Regulators and Inspectors
- Quality Management
- National Responsible Persons for Pharmacovigilance
- Heads of Pharmacovigilance