FDA Supports Innovation in Clinical Trials with eConsent

Source: Signant Health, formerly CRF Bracket

By Sandra “SAM” Sather, Quality and Regulatory, TrialConsent, CRF Health

In this short video, informed consent industry expert, Sandra "SAM" Sather, discusses the Food and Drug Administration's 2016 final guidance document for eConsent, "Use of Electronic Informed Consent."  Learn how the FDA supports Electronic Informed Consent and how it can be used to improve patient compliance and comprehension.

Signant Health, formerly CRF Bracket