Video

The Value Of Electronic Informed Consent

Source: Signant Health

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

Securing informed consent from clinical trial participants involves more than a signature—you need to ensure participants truly understand what they’re signing.  Learn from industry expert, Sandra “SAM” Sather, on how the electronic informed consent (eConsent) process improves the way participants are consented on a clinical trial.

access the Video!

Get unlimited access to:
Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of Clinical Leader? Subscribe today.

Subscribe to Clinical Leader X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.

or

Subscribe to Clinical Leader

Please tell us more about you so that we can customize our newsletters to your specific interests:

What topics interest you? (Check all that apply.)

Signant Health