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01.08.2019 back forward

New German Haemophilia Registry Online

Virtual medical data (Source: Sdecoret / Shutterstock)

On 1 August 2019 the new German Haemophilia Registry (DHR) at the Paul-Ehrlich-Institut goes online. For ten years, the DHR has been collecting therapy-relevant data from patients with haemostasis (blood coagulation) disorders, such as haemophilia A and B. Experts from the Haematology / Transfusion Medicine division have refined the database to enable it to meet the current challenges. As a result, not only can supply be monitored, but the development of new treatments can also be supported and data can be collected for research into rare diseases.

Data Collection for Optimising Treatments