Minister of Health Abdulla Nazim Ibrahim has announced plans to introduce a dedicated website and mobile application to provide online access to a national blood donor registry, as part of ongoing efforts to modernise transfusion services in the Maldives.
The update was shared in a written response to a parliamentary query submitted by North Galolhu MP Mohamed Ibrahim, focusing on improvements to blood transfusion services nationwide.
Building a National Blood Service System
According to the minister, the initiative forms part of a broader pledge by President Mohamed Muizzu to strengthen the treatment of blood-related diseases.
He said a national blood service framework has already been established, including the development of blood banks across four regions of the country. In addition, transfusion centres have been set up in 108 islands, aimed at improving access to critical services within local communities and nearby health facilities.
To support these services, laboratory technologists have been recruited, while ongoing efforts are focused on integrating operations under a unified system aligned with international standards.
Digital Transformation and Real-Time Data
The minister noted that a dedicated module has been developed within the DHIS2 system, allowing real-time access to data from transfusion centres across the country.
With technical assistance from the World Health Organization (WHO), a National Blood Standard has also been finalised, setting guidelines to improve quality and safety in transfusion services.
Registry and App Expected by October
Efforts are currently underway to digitise the existing manual blood donor registry. The ministry plans to launch a donor registry and recruitment portal, along with a mobile application, by October 2026.
The platform is expected to create a centralised database of voluntary blood donors, helping authorities respond more quickly to shortages and improve coordination during emergencies.
Thalassaemia Registry Also Established
In addition to the donor system, the minister confirmed that a national registry for thalassaemia patients has been established under the relevant legislation. Registration and data management for the system began in January 2026.
Officials say the combined initiatives represent a significant step forward in strengthening healthcare services and ensuring timely access to blood across the Maldives.
