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IDMP as a Cornerstone in Digital Transformation for Regulatory Practice in Europe
Session Chair(s)
Rodrigo Palacios, MBA
Regulatory Policy Lead
F. Hoffmann-La Roche, Switzerland
Exploring the role of IDMP in digital transformation of the regulatory process. Product data quality/availability are prerequisites to more advanced capabilities in regulatory assessments, underlying operational processes and downstream benefits.
Learning Objective : The session will identify where IDMP data can be instrumental in enabling the short-medium term operational improvement and mid-long term regulatory science transformation.
Speaker(s)
EMA Perspective
Hilmar Hamann, PhD
European Medicines Agency, Netherlands
Head of Information Management
Industry Perspective
Patrick Middag, MBA, MSc
Servier, Belgium
Principal Lead Regulatory Affairs
Industry Perspective
Emma Du Four, MBA
United Kingdom
Regulatory and R&D Policy Professional
National Regulator Perspective
Joris Kampmeijer
Medicines Evaluation Board , Netherlands
Information Processing Department
National Regulator Perspective
Frits Stulp, MSc
Iperion Life Sciences Consultancy, Netherlands
Managing Director
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