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A new drug used in a clinical investigation. The United States Food and Drug Administration's Investigational New Drug (IND) programme is the vehicle by which a pharmaceutical company is granted permission to ship an experimental drug across state lines prior to a marketing application for the drug is approved.
See also:
Food And Drug Administration (FDA)
Drug usage/utilisation review (DUR)
License (product)
Cost per thousand (CPM), Lead management, European Medicines Agency, Database marketing, Clinical trial, Effectiveness, Generic medicine, Cost–benefit analysis, Drop out, Trial endpoint, Baseline, Product pipeline, Controlled trial, Fair balance, European Federation of Pharmaceutical Industries (EFPIA),
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