Eventi
International Summer School on Rare Disease Registries and FAIRification of Data
Online registration form is available at
Further information, please visit the website at the following link:
Registries are key resources in order to increase timely and accurate diagnosis, improve patients management, tailor treatments, facilitate clinical trials, support healthcare planning and speed up research
This course is composed of two training modules:
- The first module starts on September 23 till September 25, 2019, during these three days participants will learn (a) what resources are needed for the establishment / maintenance of a high quality registry (b) the features of successful strategies to ensure (i) long-time sustainability of the registry, (ii) quality, (iii) legal and ethical issues in compliance with the EU General Data Protection Regulation and (iv) FAIR principles
- The second module “FAIRification of data”, starts on September 26 till September 27, 2019 during these two days participants, working with IT-trainers, will make use case data FAIR.The potential of a FAIR registry, as the basis for cross resource questions, will be demonstrated by executing a query across the use cases that become FAIR. In this part a time slot will be allocated to discuss FAIR data management and FAIR project planning
The training course is open to the international research community, clinicians, medical specialists, registry curators, database managers, healthcare professionals and rare disease patients representatives
Registration is possible for:
∙ the first training module (“Rare Disease Registries”, September 23-25, 2019)
∙ the second training module (“FAIRification of Data”, September 26-27, 2019)
∙ the entire course (“Rare Disease Registries” and “FAIRification of data”, September 23-27, 2019).
The draft of the programme and Logistics are available at this Link:
