International Cystic Fibrosis / Mucoviscidosis / Association (ICFMA)

Association internationale de lutte contre la mucoviscidose
Asociación Internacional contra la Fibrosis Quistica / Mucoviscidosis /

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1964-07-27 Paris France


27 Jul 1964, Paris (France), at a steering meeting; further discussion at research conference, Sep 1964, Bethesda MD (USA); first formal meeting Mar 1965, Paris. Registered in the State of Delaware, USA. Jan 2003, merged with H-XD1279 - International Association of Cystic Fibrosis Adults (IACFA) to form H-XC0133 - Cystic Fibrosis Worldwide (CFW).


Improve knowledge of cystic fibrosis among medical professionals, governments and the general public; further the interests of children and adults who have cystic fibrosis; improve medical care available to them and psychological and social care available to them and their families; stimulate, support and advance research into the nature, cause, prevention, treatment, alleviation and cure of cystic fibrosis, so as to reduce unnecessary suffering and premature death; promote establishment of national associations.


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Annual Meeting of voting (full) members. World-wide Medical/Scientific Congress (every 4 years). Officers: President; 2 Vice-Presidents: Treasurer; Secretary. Scientific/Medical Advisory Council, comprising one representative of each national association, meets every 4 years at Congress and elects Executive Committee consisting of Chairman, Vice-Chairman, Secretary and 9 other persons.


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Consultative Status

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Relations with Inter-Governmental Organizations

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Relations with Non-Governmental Organizations

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Type I Classification

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Type II Classification

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Subjects *

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UN Sustainable Development Goals **

GOAL 3: Good Health and Well-being



Last News


* Subject classification is derived from the organization names and aims.
** UN SDGs are linked to the subject classification.

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