Healthcare Information For All (HIFA) is a global campaign and community of practice of health professionals, publishers, librarians, technologists, researchers, policymakers, and patient representatives, working to improve the availability and use of reliable healthcare information worldwide.[1][2] The rationale for HIFA is described in a Lancet paper, commissioned by the World Health Organization. The paper notes that the lack of availability and use of reliable healthcare information in low- and middle-income countries is a major contributor to avoidable death and suffering, and recommends multistakeholder action to accelerate progress.[3]
HIFA was launched in October 2006 at the 10th Congress of the Association for Health Information and Libraries in Africa in Mombasa, Kenya (it was initially called HIFA 2015). It currently has more than 20,000 professional members from 2500 health and development organisations in 180 countries.[2]
^Smith, R.; Koehlmoos, T. P. (2011). "Provision of health information for all". BMJ. 342 (jun30 2): d4151. doi:10.1136/bmj.d4151. ISSN 0959-8138. PMID 21724544. S2CID 46550239.
^ ab"About HIFA | Health Information For All (HIFA.ORG)". hifa.org. Retrieved 2022-03-10.
^Godlee, Fiona; Pakenham-Walsh, Neil; Ncayiyana, Dan; Cohen, Barbara; Packer, Abel (2004). "Can we achieve health information for all by 2015?". The Lancet. 364 (9430): 295–300. doi:10.1016/S0140-6736(04)16681-6. PMID 15262109. S2CID 34056572.
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