The biggest challenge facing clinical research today is the need to gather, analyze, and report data. To collect patient data more efficiently, researchers are increasingly exploring BYOD strategies for their trials; that is, allowing patients to utilize their own devices to collect data within the context of a clinical trial.
Our white paper discusses BYOD advantages and misconceptions, regulatory, copyright, and equivalency considerations, and a Phase III case study. Read now and consider a BYOD ePRO approach for your next clinical trial.