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 incl modelling, IDMP/SPOR and Data Quality questions and on exploring AI and new digital technologies for the drug regulatory space. He has a record of successfully leading cross-functional and compliance critical, global projects and consults his business in complex process questions. With over 20 years of extensive experience in pharmaceutical industry, Joerg is an acknowledged expert in project and process management. He is a member of EMA´s IDMP/SPOR Task Force , of Allotrope and co-chair of a GAMP D-A-CH Special Interest Group on validation of AI for the regulated industry. He is a licensed pharmacist and six sigma black belt.