Run The Trial You Want
Transform clinical trials with better data collection
Life sciences companies are facing unprecedented pressure to deliver more treatments, faster, and with greater safety. All of this must be done at a lower cost to patients, caregivers, society, and even to the environment. Competition, advances in precision medicine, and impending patent expirations add further pressure to deliver more with less. In addition, there is a decline in the number of qualified sites. The race to match the patient to the trial, and the trial to the patient, is in full force. Sponsors are competing for a limited pool of patients so it is imperative they maximize each and every interaction. They must ensure that the right patient population is defined and available, and that trial objectives and activities match the expectations of patients and their primary caregivers.
In this environment, how can sponsors successfully accelerate their own development programs ahead of their competitors? The answer lies in science, and the use of prevailing theory to develop and execute the most effective study imaginable. Patients, investigators, sponsors, and regulators are some of the key stakeholders that can reap major benefits by optimizing trial design and execution. The ideal trial requires the least number of patients and runs at the shortest duration, in order to deliver results needed to confirm if a new treatment will be a success.
This paper will focus on the challenges with collecting data required for a protocol and best practices to address them. Learn how to meet the demands of modern trials with modern, cloud based electronic data capture (EDC) systems that enable you to run the trial you want.
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