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Tag Archives: OMI
Need to Reality
One of the key moments of the April FDA meeting on drug development for ME/CFS was when Bernard Munos said that ME/CFS patients will have to collect and pool their data to attract the interest of big pharma. Many advocates … Continue reading
Posted in Advocacy, Research
Tagged Biobank, CFIDS Association, data, funding, grants, networks, OMI, researchers
7 Comments