July 2022
In this edition, we will be telling you about our General Assembly meeting in Ghent, and about our work with CDISC creating paediatric data standards and much much more!
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March 2022
In the fourth edition, we will be telling you more about the c4c network especially the Norway hub, International Rare Disease Day 2022 and more!
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December 2021
In this third edition, we will be telling you more about the c4c network and how we are supporting paediatric clinical trials to ultimately improve medicines for the entire paediatric population.
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September 2021
In this second edition, we will be telling you more about the c4c network and how we are supporting paediatric clinical trials to ultimately improve medicines for the entire paediatric population.
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June 2021
In this first edition, we will be telling you more about what the c4c network is and why it is so greatly needed. The aim of c4c is to support paediatric clinical trials and ultimately improve medicines for the entire paediatric population.
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