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Plenary Session 1: Digitalisation of Clinical Data and its Support to Clinical Research
Session Chair(s)
Nick Sykes, MS
Policy Advisor, Regulatory Strategy, EFPIA, Belgium
Jesper Kjær, MS
Global Director for Public, Private Partnerships, Strat Ops, Global Med Affairs, Novo Nordisk A/S, Denmark
To remain sustainable, clinical research needs to fully embrace digitalisation. This session will take a look at how the clinical research environment is being digitalised; from how data on people’s health is being made available, to using digital technologies for the capture of data from participants in clinical trials. The session will also look at how data other than that collected in traditional clinical trials can be used to complement clinical trial data and what EU regulators are doing to prepare for this digital future.
Speaker(s)
Jerome De Barros, MS
Policy Officer - Digital Health, European Commission, Belgium
The Promise of the European Health Data Space (EHDS)
Bert Hartog, PHD, MSC
, Hartog Digital Health Consulting, Netherlands
Use of Digital Health Technologies for Capturing Clinical Trial Data – Opportunities & Pitfalls
Ana Zanoletty Perez
Head of Clinical Trials Transformation Workstream, European Medicines Agency, Netherlands
ACT EU – Supporting the Digitalisation of CTs
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