Our network
As our network grows, so does our expertise, reach, and impact. We invite researchers, clinicians, Public & Patient Involvement partners, industry members, and regulators with an interest in rare disease research to join us.
Together, we can make Ireland world-leading in patient access to rare disease research and clinical trials – shaped in partnership with the communities they serve.
Benefits of partnering with us
- Links with national and international expertise in rare disease clinical research
- Networking opportunities to build new collaborations
- Provide a platform for sharing your research activities (through our website, newsletter, social media, events)
- Capacity building and training opportunities
- Support for embedding public & patient involvement (PPI) in your research
- Support for feasibility studies and setting up a trial site
- Inclusion of your clinical trial as part of our network
How do I become a member?
1. Contact the RDCTN:
2. Start getting involved now:
Join the Community
A dedicated space to showcase your work, find collaborators, and build your profile. All are welcome - so share this with collaborators, trainees, or anyone you supervise
Stay Informed
Join our mailing list for quarterly newsletters, funding opportunities and event updates