Today, HRCI & our collaborators NISR & CFRI publish ๐๐ง๐ฅ๐จ๐๐ค๐ข๐ง๐ ๐ญ๐ก๐ ๐๐จ๐ญ๐๐ง๐ญ๐ข๐๐ฅ ๐จ๐ ๐๐๐ญ๐ข๐๐ง๐ญ ๐๐๐ ๐ข๐ฌ๐ญ๐ซ๐ข๐๐ฌ: ๐ ๐๐ฎ๐ข๐๐ ๐๐จ๐ซ ๐๐ฎ๐๐๐๐ฌ๐ฌ. It lays out practical advice on developing & sustaining a patient registry. https://t.co/BV2SrDG0Aq
Weโre excited to announce our first Annual Report will be published soon. Visit our website and subscribe to our mailing list to be among the first to receive it. https://t.co/1BPMgeDFag
We're thrilled to announce our first Annual Report will be released soon. Visit our website and subscribe to our mailing list be among the first to receive it. https://t.co/1BPMgeD7kI
As part of implementing the EU Health Data Space, @HIQA@roinnslainte@HSELive@hrbireland are creating a Public/Patient Involvement Panel on โCollecting, using, sharing health information for better services, policy, research & innovationโ Details here: https://t.co/PMAFYamT2B
The Irish EB registry is open and looking for participants, check out this great video to learn more. To register please call @CHIatCrumlin on 01-428 2646
#healthresearchmatters#EB
Today, HRCI & our collaborators NISR & CFRI publish ๐๐ง๐ฅ๐จ๐๐ค๐ข๐ง๐ ๐ญ๐ก๐ ๐๐จ๐ญ๐๐ง๐ญ๐ข๐๐ฅ ๐จ๐ ๐๐๐ญ๐ข๐๐ง๐ญ ๐๐๐ ๐ข๐ฌ๐ญ๐ซ๐ข๐๐ฌ: ๐ ๐๐ฎ๐ข๐๐ ๐๐จ๐ซ ๐๐ฎ๐๐๐๐ฌ๐ฌ. It lays out practical advice on developing & sustaining a patient registry. https://t.co/BV2SrDG0Aq
Are you a researcher interested in #EB, #Alopecia, or #Eczema? Contact us to learn more about how our Irish patient registries support research! #Skin#registries
April isย #RosaceaAwarenessMonthย -ย #rosacea is a commonย #skincondition, which mainly affects facial skin. It's most often seen in people who've fair skin & often referred to as the 'Curse of the Celts'. For more, check out our rosacea information page at:ย https://t.co/TNawUyCMDg
Thank you to all our partners, stakeholders and colleagues for joining us yesterday to mark #30YearsOfData collection, and to celebrate the launch of our 2024 โ 2026 Strategic Plan https://t.co/0xRgjjJlDO
@hseNCCP@NSShse@BreakthroCancer@cancertrials_ie
~50 people joined first meeting of Rare Disease Patient Forum. Group will feed into development of new National Rare Disease Strategy. Clear there is considerable interest amongst those living with rare diseases in this work. You can still join the group https://t.co/hsmhhXta7Z