Trialbee eConsent: Ease The Patient's Journey Into A Clinical Trial

Streamline enrollment, screening and consent with Trialbee eConsent. Designed to ease the patient’s journey into a clinical trial as well as reduce site-burden during enrollment during hybrid and decentralized trials.

With almost a decade of experience matching and enrolling patients, Trialbee is purpose-built to reduce enrollment risk and efficiently meet global clinical trial timelines. Inspired by the shift from traditional clinical trials to hybrid and decentralized clinical trials, Trialbee has developed a platform driven by datascience to optimize patient matching along with an analytics-driven approach to enrollment, simplifying the patient journey while lowering site-burden. These insights and analytics lead to tangible improvements to patient recruitment as well as enrollment strategies that accelerate clinical trial timelines and unlock operational efficiencies.

Digitize the informed consent process with a flexible eConsent workflow to ease the enrollment process and reduce both site and patient burden. Trialbee’s eConsent solution brings transparency to the clinical trial consent process and offers sites and patients the flexibility to consent to a clinical trial from the convenience of their own home while maintaining human connection and providing on-demand support. Our eConsent is fully compliant with 21 CFR Part 11 electronic signature requirements and GDPR requirements.