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5th International Summer School on Rare Disease and Orphan Drug Registries & Bring-Your-Own-Data workshop

September 18 - September 22

FREE

Registries represent key resources for Rare Disease to increase timely and accurate diagnosis, improve patients management, tailor treatments, facilitate clinical trials, support healthcare planning and speed up research. The “5th International Summer School on Rare Diseases and Orphan Drug Registries” aims to promote the establishment of Findable, Accessible, Interoperable, Reusable (FAIR) Rare Disease (RD) registries in compliance with IRDiRC and EU Recommendations. The Summer School is organized by the National Centre for Rare Diseases (ISS) in collaboration with Services and Centre for International Affairs (ISS), RD-Connect, Elixir, RD-Action, EURORDIS and endorsed by ICORD.

The Summer School will consist of plenary presentations and interactive small-group exercises, according to the Problem-Based Learning methodology. The first part of the School (September, 18-20) will provide participants with useful tools and methodologies for establish a registry, the quality of the data collected and how a registry is turned into a FAIR resource. The second part (September 21-22) will be a hands-on experience (bring your own data), where the attendees work with FAIR data experts to make their data FAIR and linkable to other data that has been made FAIR before.

PARTICIPANTS and REGISTRATION
The Summer School is open to health professionals, researchers, medical specialists, registry curators, database managers and representatives of patients associations who are involved in or intend to establish a rare disease registry, mainly inside a European Reference Network [priority will be given to Registry Curators and IT support staff, ePAG members (or a patients/patient representatives linked with ePAGs)].

The Summer School will accept max 24-27 participants. A selection process will be applied based on the participant’s background, role with reference to registry activities, and involvment in ERNs.

Registration is possible for the first part (September 18-20, 2017), the second part (September 21-22, 2017) or both. Important dates and further information at www.iss.it/cnmr.

Online registration form is available at https://it.surveymonkey.com/r/5th_Sum_School_BYOD until June 30, 2017.

FEES AND COSTS
Registration is free of charge. ISS does not cover any travel, subsistence and other costs incurred by the participants to attend the two events.

ASSESSMENT OF THE ACHIEVEMENT OF THE LEARNING OBJECTIVES
The participants’ performance will be mainly evaluated on the basis of the group work written solutions.

ATTENDANCE CERTIFICATES
At the end of the Course a certificate of attendance will be handed to the participants who attended 100% of the program. No credits of Continuing Education in Medicine will be issued.

OFFICIAL LANGUAGE
English.

VENUE
Aula Rossi, Istituto Superiore di Sanità, via Giano della Bella, 34 – 00161 Rome, Italy.

Details

Start:
September 18
End:
September 22
Cost:
FREE
Website:
http://www.iss.it/cnmr/?lang=1&id=2739&tipo=3

Organiser

FEDERG Initiative

Venue

Dravet Syndrome Foundation
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