Integrating eConsent With EDC: Streamlined Workflows For Seamless Trials

Combining electronic consent (eConsent) with electronic data capture (EDC) is transforming clinical trial operations. Traditionally, consent and data collection have been managed in separate systems, creating inefficiencies and increasing the risk of errors. By integrating these processes, research teams can maintain a single source of truth for participant information, ensuring consistency and compliance throughout the trial lifecycle. This unified approach simplifies workflows, reduces manual reconciliation, and accelerates study startup.

For patients, eConsent offers a more transparent and accessible experience, allowing them to review and sign documents digitally, while EDC ensures accurate, real-time data entry. Together, these technologies support better oversight, improve audit readiness, and enhance overall trial quality. As trials become more complex and decentralized, adopting integrated solutions like eConsent and EDC is key to driving efficiency and maintaining regulatory standards. Learn how this integration can optimize your next study.