Rare Disease Clinical Trial Network Ireland
The Rare Disease Clinical Trial Network (CTN) is a Health Research Board (HRB) – funded network that works to increase activity in rare disease clinical trials in Ireland!


The Rare Disease Clinical Trial Network collaborates with:
- Patients
- Researchers
- Industry

To support the development of:
- Rare disease clinical trials
- Trial methodology
- Researcher training

While always
Keeping the patient voice at the centre of everything they do, which leads to better quality research and outcomes that meet the needs of the rare disease community and an increase in the quantity and quality of rare disease clinical trials in Ireland.
Whether you’re a patient, researcher or industry representative, the Rare Disease Clinical Trial Network (CTN) offers opportunities to collaborate on trials and projects that can improve rare disease clinical trial design from the patient perspective and educate early career researchers on their design.
Best of all, you can explore resources and tools specifically designed for:
- Public & Patients
- Clinicians & Researchers
- Industry
- And more!
So head to their website below to see what you can discover today!


The resource shared here is an external source that Beacon had no involvement in creating. Whilst we believe this resource will be of benefit to our community, we cannot verify the accuracy, completeness, or reliability of the information provided in this resource. Sharing this resource does not imply endorsement, approval, or affiliation, nor have we received any compensation or benefit in return for sharing it. Please exercise your own judgment, and if necessary, consult with a qualified professional when relying on external information.