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Global Pharmaceutical Regulatory Affairs Summit
22-24 October 2024
Sheraton Brussels Airport, BrusselsHybrid Event

Patrick Middag
IRISS IDMP Topic Group Lead at Deloitte


Patrick has 20+ years of professional experience as an IT management professional in the pharmaceutical industry, specifically within R&D focusing on Regulatory. During this time, Patrick was also acting as vice chair of the EFPIA European Regulatory Affairs & Operations working group and as industry co-chair of the EMA SPOR task force.

As a Director at Deloitte, he is managing IT Advisory, Strategy & Governance in the Regulatory & Compliance Life Sciences practice. Current focus is on IDMP, Cloud/Technology, Data Governance & Quality. His latest project was to lead and conduct an IDMP strategy definition workshop at a Top-10 pharma customer.

Agenda Sessions

  • Multi-Stakeholder Panel: Harmonisation of IDMP Across the Globe

  • Chair’s opening remarks

  • Chair’s afternoon remarks