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A new Massive Open Online Course (MOOC) on Health Data Ethics & Regulatory Frameworks in Rare Disease Research has been launched today!
Developed as part of the European Joint Programme on Rare Diseases, in collaboration with the Rare Diseases Foundation, this course will allow you to meet clinicians, researchers, patient advocacy groups, as well as people working on European infrastructures and regulators.
You will be guided by several experts, including our FGB researchers Viviana Giannuzzi and Annalisa Landi.
It is a 4-week, free online course dedicated to undergraduates, doctoral students, health professionals, researchers and enthusiasts eager to understand the ethics and regulatory frameworks related to health data research and rare diseases.
From May 6th to June 28th, join the course for an enriching learning experience with expert educators on hand to address your queries.
Don't miss this training

opportunity: find out more and register here.

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