Events

Webinar: Grant Writing for Engaged Research

HRCI and The Wheel Logos (1200 x 300 px)

HRCI is collaborating with The Wheel to deliver an online training session on Grant Writing Tips and Tricks Date: Thursday, 19th March 2026 Time: 11.00 – 12.30 Location: Online (Zoom webinar) Register here About the session This 90-min webinar will introduce you to the fundamentals of grant writing and is ideal for those starting their […]

Do you know that equality, diversity and inclusion matter in PPI, but aren’t sure where to start?Have you ever wondered whether your PPI approach is genuinely inclusive, and what you could do to improve it? On February 25th, we’re holding a short webinar to launch a new, friendly guide to Equality, Diversity and Inclusion (EDI) in […]

HRCI HRB Joint Funding Scheme 2025/2026 Workshop

Date: Thursday, April 3rd 2025 Time: 10am – 12 noon Location: online via Zoom About the workshop If you’re interested in taking part in the next or future rounds of the HRCI/HRB Joint Funding Scheme, we would love to have you join us at an online workshop we’re hosting with the HRB on April 3rd. […]

HRCI Member Workshop: Mastering Impact Workshop completed Join us on March 13th for an interactive workshop on how to plan for, track, and communicate the impact of your research-related activities. Whether it’s the research you fund, your support for PPI, events you organise, or other research initiatives, understanding and demonstrating impact is important and valuable. […]

HRCI/HRB Joint Funding Scheme Celebration

Celebrating the funded projects under the HRCI/HRB Joint Funding Scheme On December 11th, we celebrated the latest round of health, social care and medical research projects funded by the HRCI/HRB Joint Funding Scheme in the Mansion House, Dublin 2. 12 excellent, patient/service user-focused research projects are being funded in this round of the Joint Funding […]

PPI Facilitation Workshop 7th March 2024

HRCI is inviting our member charity representatives to register for a PPI Facilitation workshop, taking place in the HRCI offices, Camden Row, Dublin 8, on Thursday, March 7th, 2024. The workshop will be taking place in person and will be a full day event, to finish at 4pm. The aim of the event is to […]

The Cystic Fibrosis Registry of Ireland, in association with Health Research Charities Ireland (HRCI), wish to invite you to an event on: The Future of Patient Registries in Ireland Date and Time: 9.30- 1.00pm, Thursday February 2nd 2023Location: Ashling Hotel, Parkgate St, Dublin 8 This in-person event will bring together stakeholders in the patient/disease registry […]

We are thrilled to announce eminent geneticist, Prof Sally Ann Lynch, as the winner of the inaugural HRCI Research Impact Award. The award seeks to highlight the impact of researchers, funded by health research charities through the HRCI/Health Research Board (HRB) Joint Funding Scheme. Sally Ann is being recognised for her work in understanding the […]

Health Research Charities Ireland along with Rare Disease Ireland, Cystic Fibrosis Ireland, IPPOSI and the Northern Ireland Rare Disease Partnership have come together to form The Rare Disease Forum. This is a public and patient involvement initiative for Ireland, North and South, which calls for coordinated action to improve the health and social care needs […]

The Rare Disease Forum (RDF) is a public and patient involvement (PPI) initiative for Ireland, North and South. The rationale for the Forum is that much more needs to be done to address the health and social care needs of those living with a rare disease in Ireland. The founding organisations and members of the […]

Events

Webinar: Grant Writing for Engaged Research

Webinar: Launching a new guide to EDI/inclusion in PPI

HRCI HRB Joint Funding Scheme 2025/2026 Workshop

HRCI Workshop: Mastering Impact

HRCI/HRB Joint Funding Scheme Celebration

PPI Facilitation Workshop 7th March 2024

The Future of Patient Registries in Ireland

Winner of the first HRCI Research Impact Award announced

Rare Disease Forum-Partnering to Advance the Rare Disease Agenda

Rare Disease Forum 2022