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The RD-Connect Sample Catalogue is available now at samples.rd-connect.eu.
The label highlights resources of fundamental importance to the international rare diseases research and development community.
An article on the role of RD-Connect in rare disease research has been published in the Spanish online magazine Diario Medico. The article is based on the interview with Sergi(…)
The magazine Pan European Networks Health published an interview with RD-Connect focusing on the role of biobanks and how RD-Connect links them up to facilitate in rare disease research.
EURORDIS has published a webinar explaining how RD-Connect supports rare disease research and benefits patients.
The official name of the genomics platform is now Genome-Phenome Analysis Platform, while ID-Cards has been renames to Registry & Biobank Finder.
We are pleased to announce that the next RD-Connect Annual Meeting will take place on the 16-18th April 2018, in Athens, Greece.
We have launched a new version of the RD-Connect website. As well as a new look, the website also has some new content and features.
The focus on Public Private Partnership (PPP) emerged as PPPs are strongly endorsed as a model by EU grant funding schemes.
The nominations for the EURORDIS Black Pearl Awards 2018 are now open. Nominate a Rare Disease Star of 2018 today! The Awards strive to recognise the exceptional accomplishments and groundbreaking(…)
The International Rare Diseases Research Consortium (IRDiRC) has announces the new vision and goals: enable all people living with a rare disease to receive an accurate diagnosis, care, and available(…)
We would like to congratulate Joanna Vella, the RD-Connect partner at the University of Malta, who won the JRC Malta Young Scientist Award in the rare diseases field!
Register to the Summer School and/or Bring-Your-Own-Data workshop in Rome in September!