Rare Kidney Disease Registries: From Patient Data to Drug Development

2 Apr 2027 09:15 10:45
Ballroom 2
Time Session
09:15
09:37
How have rare kidney disease registries transformed clinical development?
09:37
10:00
From registry to regulatory evidence: how RaDaR works
10:00
10:22
Building a national disease registry: lessons from the Japanese Paediatric Alport Syndrome Registry
10:22
10:45
Q&A