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As clinical trials have become more complex and expensive to conduct, clinical professionals have increasingly sought new technologies to proactively and productively manage patients, site, depots, and clinical supplies on a global basis. Adaptive and other dynamic designs require clinicians to respond quickly based on data relating to patient dosing, adverse effects, laboratory results, and other study factors. Changes need to be made quickly to remain compliant with the protocol and maintain the study timeline. And with expensive drugs, such as certain biological entities, it is important to manage expiry efficiently to adhere to budgets and assure there’s supply at the site for patient visits. DRIVE was developed to help clients overcome these types of clinical trial challenges.

Download our brochure to learn how DRIVE’S advanced features, functionality, and reporting can help you productively and proactively manage clinical supplies globally — all from one portal.

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