The European Joint Programme on Rare Diseases just pre-announced the Joint Transnational Call 2022, a funding opportunity for research projects on the development of new analytic tools and pathways to accelerate diagnosis and facilitate diagnostic monitoring of rare diseases.
The EJP RD Research Mobility Fellowships funding opportunity is open until November 28. The call aims to support PhD students, Postdocs and medical doctors in training to undertake scientific visits fostering specialist research training outside their countries of residence.
The European Biotech Week comprises a weeklong series of events celebrating biotechnology, an innovative and vibrant sector launched by the discovery of the DNA molecule back in 1953. The first European Biotech Week that took place in 2013 marked the 60th anniversary...
We are excited to announce a paper about the recently formed International Hemologlobinopathy Research Network – INHERENT, published in the American Journal of Hematology.
The first European Joint Programme on Rare Diseases – EJP RD MOOC (Massive Open Online Course) “Diagnosing Rare Diseases: from the Clinic to Research and back” has started on Tuesday April 27th, 2021.
c4c network has announced that the first site is now open to recruitment for the “Kawasaki Disease Coronary Artery Aneurysm Prevention trial (KD-CAAP)” study, that is the first, of the proof of viability studies, to begin recruitment.
The European Joint Program on Rare Diseases (EJP RD) was pleased to announce its second General Assembly (GA) and Consortium Meeting, which took place from 14 to 18 September 2020 online, due to the COVID-19 crisis at the time. The EJP RD brought together over 130...
The ARISE webinar series on Sickle Cell Disease continues. The webinar “Newborn Sickle Cell Disease Screening“ has been organised and it will be held on Wednesday 22nd July, 2020 at 05:00 PM (BST).
An online meeting, open to all c4c consortium members, was organised on 24th June 2020 to present the achievements reached so far and the next steps related to data coordination and quality standard tasks. It was an occasion to have a series of talks, demonstrations and interactive sessions of the Information Technology (IT) tools that are under development.
Lately, a set of webinars focused on Sickle Cell Disease have been organised within the ARISE project. A new one will be held on 24th June 2020 at 03:30 PM BST and will address the paediatric to adult transition care for patients with sickle cell disease.
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