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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)
Related terms
Concordance programme, Market challenger, Gatekeeper, Internal Customers, Pharmaceutical Pricing Regulation Scheme (PPRS), Behavioural targeting, Launch plan, Treatment trials, Marginal analysis, Normal distribution, Marketing decision support system (MDSS), Loss leader, Defined daily dose (DDD), Product attributes, Ad impression,
