Watch the video on REDgistry!
Watch the video on REDgistry!
The European Rare Eye Disease Registry “REDgistry” is the European patient registry for all rare eye diseases. REDgistry is intended to facilitate the development of epidemiological studies, boost research, enable the identification of patients who still lack diagnosis and facilitate the preparation of cohorts for clinical trials. As of July 2023, the first patients have […]
READ THIS NEWSERN-EYE has been funded to build the basic registry for rare eye diseases named: REDgistry. The proposal submitted in September 2019 has received the positive reply from the European Commission end of January 2020…
READ THIS NEWS