We’ve rethought the process. So you can leave paper—and complexity, and patient confusion, and site frustration, and unnecessary expenses—behind.

Bioclinica eConsent is built for the way clinical trials are run today, turning a regulatory checkbox into a powerful tool for engagement that can speed study completion.

  • Patients get easy-to-understand, engaging content
  • Sites get easy-to-deploy tools that can boost retention
  • CROs and sponsors get enhanced functionality and streamlined implementation
  • IRBs get to see the actual patient process to help accelerate approvals

Stop converting long, boring paper documents into… long, boring digital documents. Start implementing an approach that makes the process of eConsent—and the process of getting it up and running—smarter, faster, more effective and more affordable. Download the Bioclinica eConsent fact sheet now.

View Resource