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Global Pharmaceutical Regulatory Affairs Summit
28-30 September 2026
Radisson Brussels Grand PlaceBrussels

Matthias Sijtstra
Senior Consultant at MAIN5
Speaker

Profile

Matthias is a Senior Consultant at MAIN5, specializing in regulatory data management, RIM implementations, and compliance initiatives such as IDMP. He helps pharmaceutical companies look beyond compliance by connecting people, processes, data, and technology to improve data quality and regulatory processes. Matthias holds an MSc in Regulatory Affairs and is particularly interested in how data governance, FAIR principles, ontologies, and knowledge graphs can make regulatory information more connected, reusable, and valuable across the organization.

Agenda Sessions

  • Beyond the IDMP Deadline: Why Product Data Only Stays Good if Someone Uses It

    13:30