Registration

The RE(ACT) – Rare Disease Research Congress is a non-profit event that promotes rare disease research and fosters stakeholder collaboration. All registration fees are dedicated solely to covering the costs of organizing the congress, and no profit is made.

Please read the General Terms and Conditions carefully

Registration fees (prices are in Euro):

• Early registration (opens April 2026): before June 30, 2026
• Standard registration: between July 1 and December 31, 2026
• Late and on-site registration: from January 1 to February 28, 2027
• Abstract submission deadline: January 31, 2027

* Our conference secretariat will verify your membership (applicable only for public/not-for-profit institutions).

** Please e-mail a copy of a Student’s ID or a confirmation signed by the department head at the time of registration. Confirmations handed in at a later stage cannot be considered.

*** Please e-mail a confirmation signed by the head of the organization at the time of your registration. Confirmations handed in later cannot be considered.

Prices are in Euro (payment by credit card with Stripe is charged with a fee of 3,5%)

The registration fee includes:

• Access to all sessions, lunches, and coffee breaks
• Access to the Opening Session
• Access to the Social Event
• Endless opportunities to network with colleagues
• Online Congress Program Guide and Abstract Book