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EHA remembers Tessa Holyoake
The Hague, September 2017
We received the sad news of Professor Tessa Holyoake’s passing. Tessa Holyoake was a Professor of Experimental Hematology and the Head of the Paul O'Gorman Leukemia Research Centre.
Poster presentation instructions
Poster Presentations will be presented as a paper poster in Madrid, as well as uploaded as an e-poster in the Congress platform.
Read moreCall for urgent action on medicine shortages in Europe
Medicine shortages are an increasing problem across Europe, posing a severe threat to patient outcomes and patient safety. In a new position paper the European Public Health Alliance (EPHA) presents nine recommendations for addressing the shortages crisis.
Read moreHematology Tutorials
Hematology Tutorials are courses aiming to provide laboratory and clinical hematologists with an integrated diagnostic and clinical work-up of hematological disorders.
Read moreHow to apply for CBTH
TimelinesApplication CBTH 2025
Deadline: August 30, 2024 (12:00 CEST)
Notification
November 2024
How to apply?Download the signature letter template. Fill in the template and get it duly signed for upload into the online application platform.
How to apply
The CRTH 2025 call for applications are open. Apply now
Timelines
Application CRTH 2025
Deadline: August 30, 2024 (12:00 CEST)
Notification
November 2024
Questions: training@ehaweb. orgDownload the Signature letter template.
EHA-Balkan Hematology Day 2023
EHA is joining forces with the national societies from the Balkan countries and co-organizing with them the 4th edition of the EHA-Balkan Hematology Day.
Read moreSecond EHA-SAH tutorial in Argentina, another success
Hematologists from South America and mainland US gathered in Argentina on September 14-15 for brain-stretching exercises on the topics of lymphoid malignancies and plasma cell dyscrasias.
Read moreFDA Reports of Secondary Malignancies Following Chimeric Antigen Receptor (CAR) T Cell Therapies and Relative Risk: an EBMT-EHA-GoCART Coalition Statement
We need to bring your attention to the recent warning disseminated by the Food and Drug Administration (FDA) regarding T-cell lymphomas in patients undergoing Chimeric Antigen Receptor T-cell (CAR-T) therapy (1).
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