A regulation in the US which attempts to give seriously ill patients access to new developmental drugs as early as possible. These drugs are generally made available during phase III studies before general marketing begins.
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Treatment Investigational New Drug (IND)
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In-house newspaper/magazine, Decision flow diagram, Marketing myopia, Prior approval, Inclusion/exclusion criteria, Side-effects, Health technology assessment/appraisal (HTA), “P” Medicine, Market growth rate, Omnibus survey, Publics, Market entry barrier, List building, Substantiation, Logo,