The World Federation of Hemophilia (WFH) publishes internationally recognized guidelines to support the care and treatment of people with inherited bleeding disorders.
This hub is home to the WFH’s Living Guidelines for the Management of Hemophilia, which are
continuously updated in response to new evidence, therapies, and evolving clinical practice. As a “living” resource, these guidelines evolve over time to reflect the most current evidence.
The living model also includes:
The Guidelines Hub also hosts WFH guidelines for the
treatment of von Willebrand disease (VWD):
Glenn Pierce, MD, PhD
WFH Vice President, Medical
The World Federation of Hemophilia has published the third edition of Guidelines for the Management of Hemophilia. Developed through a formal evidence-informed and consensus-based methodology involving multidisciplinary healthcare professionals (HCPs) and well-informed people with hemophilia (PWH), these guidelines offer 340 practical recommendations on managing care for PWH. The guidance provides a framework for the development of a comprehensive healthcare system supporting PWH, including advocacy and patient empowerment.
These materials are derived from the WFH Guidelines for the Management of Hemophilia, 3rd edition [© 2020 World Federation of Hemophilia. Haemophilia © 2020 John Wiley & Sons Ltd]
For the full set of recommendations, please refer to the full WFH Treatment Guidelines, available here.
For questions, contact treatmentguidelines@wfh.org
These educational materials were made possible through the support of the Hemophilia Alliance.
© World Federation of Hemophilia 2025