This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.

Global Pharmaceutical Regulatory Affairs Summit
21-23 October 2025
Hotel Palace BerlinBerlin, DE

Laurent Desqueper
IT Regulatory Affairs & QA at UCB
Speaker

Profile

  • Recently joined UCB as IT Expert Regulatory Affairs & QA
  • 10 years at MSD, as Business Lead for XEVMPD, IDMP (SPOR) and PLM (Web eAF) as part of the Digital Strategy at MSD
  • 15 years of IT Consultancy at TRASYS to work on projects for various departments of the European Commission, and for several European Patent Offices; with a focus of 10 years working for the European Medicines Agency on topics including eCTD, EU Module 1, Reference Data Model (RDM), Adverse Events, Product Information Management (PIM)…
  • Although these years, Laurent has a strong policy presence as Industry Subject Matter Expert for the IDMP/PMS Working Group, as member of the EFPIA ERAO-IDMP Working Group, as well as in ICH (M2, E2B and M4Q)

Agenda Sessions

  • Implementation in Europe

    08:40