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Global Pharmaceutical Regulatory Affairs Summit

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28-30 September 2026
Radisson Brussels Grand PlaceBrussels

Patrick Middag
Principal Regulatory Affairs Lead, HRIM Program at Servier
Speaker

Profile

Patrick has recently rejoined the pharmaceutical industry, working for SERVIER. He’s a Principal Regulatory Affairs Lead and program workstream leader on the company’s strategic RIM transformation program. His focus is on alignment of business processes, data and organisation to maximize business value & benefits. In parallel, he is externally engaged as the company’s representative on a few EFPIA working groups. Patrick has more than 20 years of experience in the industry, most notably at Bristol-Myers Squibb, where he was a global lead of the IDMP programme, vice chair of EFPIA’s ERAO and an active member of the SPOR Task Force.

Agenda Sessions

  • Track Chair’s Opening Remarks

    13:45
  • IDMP Readiness - Practical Implementation Strategies

    15:30
  • Resource Optimization Strategies and Digital Transformation - Closing the Adoption Gap

    11:35