• Global QPPV challenges
• Trends requiring QPPV awareness
• Impact of modern technology on the field
• AI and Digitalisation
• Harmonisation
• Impact of new local requirements for international Qualified Persons (QPs).
• Local QPPVs network
• Data privacy
• Globalising the PSMF – Tool for Global Understanding
• Interaction Between the Different Local QPPVs (EU and non-EU) and the EU QPPV
• QPPV Oversight
• Inspections

• QPPVs and Deputies from any territory
• Regulators
• Pharmacovigilance Consultants
• Directors of Pharmacovigilance Oversight and Standards
• Drug Safety Managers/ Leaders
• Auditors
• Medical and Regulatory Affairs Experts
• Aspiring PV Specialists/QPPVs
• QPPV Support Staff

The DIA Global QPPV Forum is the premier platform designed exclusively for QPPVs to engage in meaningful exchanges. Bringing together professionals from diverse backgrounds, including small to large pharmaceutical companies and consultants, this forum offers unparalleled networking opportunities.

Attendees benefit from direct access to regulators and inspectors, facilitating valuable interactions and discussions. The agenda includes new topics such as the evolving role of QPPVs in different organisational settings (big pharma, small pharma, CROs), as well as insights into QPPV requirements and expectations in non-EU countries.

• Upon completion, learners should be able to:

  • Hear the latest updates and hot topics relating to the role of QPPV
  • Explore long-term PV visions, future directions of the the future directions of the ‘PV world’ and potential impact on the role of the QPPV
  • Network with colleagues and meet regulators
  • Learn from and share experiences and ideas with like-minded QPPVs in a neutral environment
  • Better uderstand regulatory and inspectorate expectations globally
  • Examine current challenges and share potential solutions