12.06.22 -- Empowering The Use Of eConsent

The proliferation of both patient-centric and hybrid clinical trials has created a need for more individualized, simplified, accessible processes involving trial participants. Learn how eConsent digitalizes the trial participant consent process through increasingly simplified models designed to improve comprehension and boost engagement.

The clinical research industry has been reluctant to adopt eConsent for several reasons, not least of which included having to disrupt already stressed and short-staffed work environments to implement new technology. Read how the industry should continue exploring and implementing digital technologies in earnest.

Technology is critical to clinical trial efficiency and data quality, particularly for supporting the increased operational complexities of research. But it often misses the mark when it comes to integrating them into the clinical trial workflow. Discover ways to think broadly about the effective implementation of technology.