ERN-Skin
ERN-Skin is the European Reference Network for Rare and Undiagnosed Skin Disorders
ern-skin.eu
24/09/2026
📢 2026 ERN-Skin Board Meeting
We are pleased to announce that the next ERN-Skin Board Meeting will take place on 19–20 November 2026 in Paris, France.
📍 The meeting will be hosted at Hôpital Necker–Enfants Malades and Institut Imagine.
đź“„ The preliminary programme is now available. Discover the planned sessions and activities and start preparing for the meeting:https://ern-skin.eu/wp-content/uploads/2026/09/2026-Board-Programme-15092026.pdf
We look forward to welcoming the ERN-Skin team to Paris! 🇫🇷
10/09/2026
📢 Little reminder: the deadline is TODAY!
We’re sharing this opportunity with you one last time: the ERDERA Clinical Trial Call 2026 (ECTC) is open for applications, with the Expression of Interest deadline today, 10 September 2026.
The call supports multinational, GCP-compliant early-phase clinical trials in rare diseases, including Phase I, Phase I/II and Phase II studies, with the aim of strengthening clinical evidence and accelerating the development of innovative treatments.
If you or your colleagues are working on rare disease clinical research, today is the last opportunity to submit an Expression of Interest.
👉 More information: https://erdera.org/call/ctc2026/
Please help us spread the word by sharing this opportunity with your network! đź’™
Erdera
Clinical Trial Call - ERDERA ERDERA has launched its Clinical Trial Call (ECTC) to support multinational, GCP‑compliant early‑phase interventional clinical trials in rare diseases.
08/09/2026
⏳The ERN-Skin Symposium is coming soon!
We’re getting closer to the 2026 EADV Congress, where we’ll be hosting the ERN-Skin Symposium on 30 September 2026, from 8:30 to 10:00 CEST.
Join us for a morning of knowledge sharing, discussion and exchange around rare skin diseases.
Have a look at the program of the session: https://pagv3.virtual-meeting.org/eadv/eadvcongress2026/en-GB/pag/session/6858?is_sponsored=-1&view=vertical&segment=sessions&fullscreen=1
We look forward to seeing you there!
EADV - European Academy of Dermatology and Venereology
24/08/2026
Making information more accessible can make a real difference. 🌍
Today, we would like to highlight the work of CMTC-OVM, a global non-profit patient organisation supporting patients and families affected by vascular malformations.
CMTC-OVM provides a valuable collection of information folders in multiple languages, covering a wide range of conditions and topics relevant to patients, families, caregivers, teachers and healthcare professionals.
For people navigating a rare condition, access to understandable and relevant information is an important part of feeling informed, supported and less alone.
We invite you to explore these resources and share them.
🔎 Find the information folders on the CMTC-OVM website: https://www.cmtc.nl/en/activities/information-material/information-folders/
Information folders CMTC-OVM Netherlands We have a whole series of information folders available in multiple languages. All folders can be downloaded or sent directly!
27/07/2026
đź’» Register to our upcoming ERN-Skin AIBD Webinar!
📆 Taking place on 30th of July 2026 from 5:00 – 6:00 pm CET
Organized by the ERN-Skin AIBD thematic group this webinar will be structured into 2 parts:
🔹 Part 1: Over-mortality in bullous pemphigoid patients in the first 6 months after diagnosis: insights from a cohort study, presented by Carmen Glück, Würzburg.
🔹 Part 2: Drug survival in bullous pemphigoid, presented by Leon Johannsen, Würzburg.
It will be chaired by Marc Yale, Research & Policy Advisor at International Pemphigus & Pemphigoid Foundation.
👉 If you haven't registered yet, make sure to register: https://ern-skin.eu/webinars/
09/07/2026
✨ A wrap-up of Day 1 at !
Today was filled with inspiring talks, the latest research, engaging discussions, and plenty of opportunities to connect with colleagues working across the rare skin disease community.
It was great to see researchers, clinicians, patient representatives, and industry partners exchanging ideas and sharing experiences throughout the day.
We are looking forward to another day of learning, collaboration, and conversations that continue to drive progress in rare skin diseases.
See you tomorrow! đź‘‹
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