The Haemophilia Foundaon of Nigeria maintains a bleeding disorder registry that serves as a plaorm for the Haemophilia Treatment Centres (HTCs) across the country to present and collect uniform and standardized paent data. This data is used to guide clinical pracce and improve care for those affected. As an organizaon with at least 15 HTCs in government hospitals and medical praconers in fields applicable to the care and management of people with bleeding disorders...