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

Jörg Stüben
Head of Regulatory Information Management and Senior Expert at Boehringer Ingelheim International GmbH


Dr Joerg Stueben works as “Head of Regulatory Information Management and Senior Expert” for Boehringer Ingelheim. He oversees all typical activities of a RIM group with a focus on Data Management, IDMP/SPOR and Data Quality questions. He has a record of successfully leading cross-functional and compliance critical, global projects and consults his business in complex process questions. With over 25 years of extensive experience in pharmaceutical industry, Joerg is an acknowledged expert in project and process management. He was a member of EMA´s IDMP/SPOR Task Force until it was discontinued and is a member of the GAMP-DACH Steering Comittee. He is a licensed pharmacist and six sigma black belt.

Agenda Sessions

  • Chair’s opening remarks

  • EMA’s Agile Transformation: A Multi-Stakeholder Perspective

  • Chair’s afternoon remarks

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

  • Industry Case Study: Regulatory Cloud Capabilities