CDH International is proud to introduce the new CDH Patient Registry! Our natural history study database has been updated to a REDCap server and our organization is working with The …
The CDH Patient Registry is LIVE – Participate in Research!
CDH International Speaks At Bio Data World Congress 2020
CDH International participated in the Bio Data World Congress 2020 last week. Our President, Dawn Ireland, spoke on how our grassroots patient organization started our own natural history research database and …
