The Essential Guide to Electronic Informed Consent

November 16, 2016

Informed consent is more than just a form – it's a process.

Regulators and industry groups are pushing for the adoption of electronic informed consent (eConsent) for the multitude of benefits it offer patients as well as sponsors and site teams, but the technology is so new, it can be hard to know where to start.

Download our latest eBook, "The Essential Guide to Electronic Informed Consent," to learn how eConsent enhances the consent process by: 

 

  • Streamlining the process for real-time access to patients/study teams 
  • Designing the electronic consent to support adult learning
  • Enhancing regulatory compliance to reduce risks
  • Saving sponsors time and money
  • ...And more!

 

Previous Guide
TrialConsent Product Overview
TrialConsent Product Overview

Introducing an eConsent solution that makes digitizing the consent process easy at any scale. Use TrialCons...

Next Flipbook
TrialConsent for IRBs and ECs (Ethics Committees)
TrialConsent for IRBs and ECs (Ethics Committees)

Discover the value of TrialConsent (eConsent) for IRBs and Ethics Committees by Signant Health.