Electronic Informed Consent in Clinical Research

White Paper

Electronic Informed Consent in Clinical Research

Medidata is conducting a study to understand the regulatory positions, adoption and the variability regarding eConsent globally.  The benefits of eConsent have been well documented, yet there is still concern and uncertainty around regulatory positions.  This white paper is the first in a series to provide an overview of findings from the Medidata eConsent study, which includes the most recent feedback and guidance from relevant regulatory bodies.