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EHA Friends' Fund

Together, we can change the lives of many and make greater strides in the treatment of patients with blood disorders.

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New data exchange platform on rare diseases

The European Commission (EC) launched a new online knowledge-sharing platform – the European Platform on Rare Disease Registration (EU RD Platform) – on February 28, 2019.

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Healthcare-affiliated professional membership

You don't need to be scientific researcher or a physician to join our vibrant community.

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EHA Research Grant review and selection process

1. Eligibility checkAfter the deadline has passed, we'll check your application for completion and compliance with the eligibility criteria.

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