Abstract
This article describes the results of a survey of formulary managers regarding policies and practices relevant to biotechnology medicines. The objectives of the survey were to 1) classify major strategies for controlling current expenditures on biotechnology drugs within managed care plans, 2) categorize their future strategies, and 3) identify the perceived effectiveness of strategies currently in use. Results from the survey suggest that the evolving sophistication of formulary management is a major factor that must be taken into consideration early in clinical research efforts, as well as in the design of clinical trials. Drug Dev.
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