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Code of Ethics

Widely acknowledged as the global voice of thalassaemia patients, TIF needs funds to carry out its mission to advocate and support the development and implementation of control programmes for thalassaemia, including prevention and clinical management.

TIF’s funding derives from a number of sources including international and regional funds, industry, generous donors, organisations in the pursuit of their common interest in haemoglobin disorders (thalassaemia and sickle cell disease).

The overall proportion of industry related funding is 46.74% and the non-industry funding is 53.26%. The highest contribution from a single company is 17.71%.

Documentation

As a patient-driven organisation, TIF is committed to maintaining its independence and will make choices and take positions based solely upon patients’ needs and perspectives.

Our Supporters

TIF’s work may attract the attention of public and private institutions, foundations and other bodies, as well as companies or industry representative organisations which have a particular interest in the development of drugs, medical equipment, consumables and other medical and healthcare related products and technologies.

Our Supporters