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Menu
Home
About Us
Our Work
Joint Funding Scheme
Advocacy
Member Support
Patient & Public Involvement (PPI)
IHRF
Patient Registries
Rare Diseases
Intellectual Property
Working With Industry
Our Staff
Our Board
Board Meetings
Governance
Annual Reports
Audited Accounts
Privacy Policy
Contact Us
Research Funding
How It Works
Timeline
Open Calls
Scheme Impact
Testimonials
Past Rounds
Project Examples
Membership
Our Members
Full Membership
Associate Membership
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Membership Enquiry form
News & Events
HRCI Events
IHRF Events
Other Events
Blog
Videos
Publications
Latest Publications
Position Papers & Advocacy
Patient & Public Involvement
Research governance & Funding
Rare Diseases
Health Information
Annual Reports
IHRF
IHRF Steering Group
IHRF Terms of Reference
IHRF Events
Menu
Home
About Us
Our Work
Joint Funding Scheme
Advocacy
Member Support
Patient & Public Involvement (PPI)
IHRF
Patient Registries
Rare Diseases
Intellectual Property
Working With Industry
Our Staff
Our Board
Board Meetings
Governance
Annual Reports
Audited Accounts
Privacy Policy
Contact Us
Research Funding
How It Works
Timeline
Open Calls
Scheme Impact
Testimonials
Past Rounds
Project Examples
Membership
Our Members
Full Membership
Associate Membership
Membership Criteria
Membership Enquiry form
News & Events
HRCI Events
IHRF Events
Other Events
Blog
Videos
Publications
Latest Publications
Position Papers & Advocacy
Patient & Public Involvement
Research governance & Funding
Rare Diseases
Health Information
Annual Reports
IHRF
IHRF Steering Group
IHRF Terms of Reference
IHRF Events
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Publications
Our most recent documents.
June 25, 2020
A new PPI toolkit
June 9, 2020
Launching our 2019 Annual Report
February 27, 2020
An Easyguide to Rare Diseases in Ireland and Consensus for Action
December 5, 2019
Report: Do patients and the public trust researchers with their health data?
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