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About
About ERDERA
Rare Disease Dashboard
Beneficiaries and Participants
Structure and Governance
Who we are
Science to policy
Living with rare
Research Services
Funding
Clinical Research Network
Data Hub
Expertise services
Erdera accelerator
Training and education
International Alignment
Latest
News & articles
Events
Knowledge Pills
Publications
Multimedia
Resources
Events Calendar
ERDERA Learning Portal
RD Virtual Platform
Innovation Management Toolbox (IMT)
Rare Diseases Clinical Trials Toolbox
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Ireland
Your Tag: Ireland
Launching a New Guide to EDI/Inclusion in PPI
26 January 2026
February 25
@
1:00 pm
-
2:00 pm
A short webinar to launch a new, friendly guide to Equality, Diversity and Inclusion (EDI) in Public and Patient Involvement (PPI).
State of the Art 2025 RD Report: Ireland
26 September 2025
This 2025 country report outlines the policy, research, care and support landscape for rare diseases in Ireland.
“There’s a lot of value in connecting with other countries — learning what has worked, what hasn’t, and applying those lessons”
11 June 2025
ERDERA interviews Gavin Lawler co-ordinates the Irish National Mirror Group (NMG) on rare diseases as Programme Manager within the Health Research Board Ireland.
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About
About ERDERA
Rare Disease Dashboard
Beneficiaries and Participants
Structure and Governance
Who we are
Science to policy
Living with rare
Research Services
Funding
Clinical Research Network
Data Hub
Expertise services
Erdera accelerator
Training and education
International Alignment
Latest
News & articles
Events
Knowledge Pills
Publications
Multimedia
Resources
Events Calendar
ERDERA Learning Portal
RD Virtual Platform
Innovation Management Toolbox (IMT)
Rare Diseases Clinical Trials Toolbox
ERN consent forms
Contact Us