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The European Conference on Rare Diseases & Orphan Products (ECRD) 2026 will take place on 3 – 4 June 2026 in Prague, under the title “Rare Diseases in a Changing & Competitive Europe: Shaping policies to address the unmet needs of people living with rare diseases”. The conference will be held in a hybrid format and will provide a unique platform for connection and collaboration across the rare disease community. It will bring together patients, advocates, policymakers, healthcare industry representatives, clinicians, regulators, and Member State officials to discuss, shape, and advance goal-driven policies that improve the lives of people living with rare diseases and their families. CCI Europe is proud to be an associate partner of the conference.

The European Conference on Rare Diseases & Orphan Products (ECRD) is the largest patient-led policy-shaping event on rare diseases in Europe. By bringing together people living with rare diseases and patient advocates alongside policymakers, healthcare industry representatives, clinicians, regulators, and Member State officials, EURORDIS leverages the strength of this unique network to advance goal-driven policies that improve the lives of people living with a rare disease and their families.

ECRD 2026 is expected to unite over 500 participants in Prague, with an additional 300+ joining online. Thanks to its hybrid format, the conference will provide an unparalleled platform for connection and collaboration, enabling participants across the rare disease community to exchange knowledge, share experiences, and build partnerships.

ECRD 2026 will also mark the launch of a multi-stakeholder process to develop a European Action Plan for Rare Diseases. Through open dialogue, participants will help shape a roadmap that defines shared priorities, structure, governance, funding, and delivery mechanisms.

This collaborative process will ensure collective ownership and lasting impact across Europe, while strengthening Europe’s role as a key contributor to the WHO Global Action Plan on Rare Diseases.

The event will delve into the most pressing discussions on the future of Europe and medicines, exploring the multifaceted challenges and opportunities for the rare disease ecosystem. The programme will cover a broad range of policy topics, including therapy development, timely and accurate diagnosis, advances in social sciences, specialised healthcare, and health technology assessments.

By participating in ECRD 2026, you will play an active role in shaping the future of rare disease policy in Europe and beyond—helping to drive real, lasting change for millions of people living with a rare disease.

ECRD 2026 Tracks

Please see below for more information about the ECRD 2026 Tracks. Each track will contain two 90-minute, content-filled sessions, and sessions will be run in parallel, with three taking place at a time.

  • Therapies, development, and access
  • Diagnosis, research, and prevention
  • Social sciences and holistic care
  • Specialised healthcare
  • HTA (Health Technology Assessments)
  • Mental health, social and holistic care

Important Dates

  • Poster abstract submissions: 6 March 2026 – learn more and submit your abstract here.
  • Event Dates: 3-4 June 2026

Details

Start:
June 3
End:
June 4
Event Tags:
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Website:
https://www.rare-diseases.eu

Venue

Prague

Organizer

EURORDIS-Rare Diseases Europe
View Organizer Website

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