×

Premium Content - Please Submit to Continue:

First Name
Last Name
Company
Thank you!
Error - something went wrong!
   

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
INFOGRAPHIC: 14 Drivers of eConsent Adoption in Clinical Trials
INFOGRAPHIC: 14 Drivers of eConsent Adoption in Clinical Trials

Next
3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent
3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent

×

Request a TrialConsent Demonstration:

First Name
Last Name
Company
Thank you, we'll talk soon!
Error - something went wrong!