Until recently, sponsors and CROs engaged their central
laboratory simply for routine safety testing. However, as clinical trial
protocols have grown in complexity expert consultation in diagnostic
testing at the beginning of protocol development is fast becoming
critical to optimize test selection and match clinical diagnostic
endpoints to outcomes.
This e-book explores how collaborating with
your central lab partner early in protocol development can help optimize
clinical trials, drive efficiencies, avoid potential protocol
amendments, and minimize costly study delays.
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