Kicking Off A Clinical Trial The Right Way - With Seamless Digital Consent

While clinical trials have historically required participants to travel to physical sites multiple times over the course of a study, a growing focus on patient-centricity and recent global health events have transformed clinical trial conduct, accelerating the adoption of flexible technology options to support clinical trial recruitment and enrollment.

Today’s clinical trials have the ability to leverage telemedicine, electronic consent (eConsent), and other technology-mediated communications within a framework of decentralized clinical trial (DCT) to conduct personalized interactions that improve participants’ understanding and retention, while streamlining workflows, enhancing data quality and compliance, and increasing transparency with real-time reporting and insight.

Read on to learn more about how eConsent can enhance participant engagement and retention when used both onsite and remotely.