When: November 23, 11:00 EDT / 16:00 BST / 8:00 PDT / 24:00 JST
This webinar will explore why the FAIR data principles are so important for data that is collected during rare and paediatric clinical trials. We will introduce the conect4children (c4c) project and present the network that has been established under the IMI2 grant. c4c has a number of interesting tasks around the harmonisation of clinical trial data including the development of a paediatric data dictionary, a Paediatric User Guide (developed in collaboration with CDISC) and activities exploring the connectivity between real world data and paediatric clinical trials. At the heart of all of c4c’s data harmonisation efforts are the FAIR data principles, and the challenging task of applying FAIR to data collected at the CRF (or patient) level. This webinar will present the approach c4c is taking to FAIRification, the collaboration with FAIRPlus and how we plan to tackle the harmonisation of disease specific data. We are planning an interactive webinar with lots of opportunity for questions and discussion. We hope you will join us.
Project manager at conect4children
Rare Disease Policy Manager at Newcastle University
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