What is eConsent?

A powerful tool for researchers

Electronic informed consent (eConsent) refers to the use of electronic systems to convey information related to a study and to obtain and document informed consent.

> Read our recent blog posts on eConsent

> FDA guidance on use of electronic informed consent

Quorum Review IRB has reviewed eConsent solutions from every major provider and will continue to accept submissions from other vendors.

Overcoming paper-based research headaches

eConsent is a powerful tool available to researchers that offers improved participant engagement, reduces consent documentation errors, and ensures compliance and security. This is why more and more researchers are incorporating eConsent solutions into their trials.

View our free webinar on-demand:
> How eConsent Optimizes Research for Sponsors and CROs