Enabling Electronic Informed Consent for Clinical Research Sites

July 24, 2019

Securing informed consent from clinical trial participants involves more than a signature. Effective informed consent ensures your participants truly understand what they are signing. Effective electronic informed consent  provides user friendly tools to guide them along the way.

Watch this information session on eConsent designed exclusively for clinical research sites to see first-hand how your site can be ready for eConsent. In this education-focused session, learn the benefits of eConsent, technology options and features, and implementation best practices.

Did You Know?

  • 77% of sites think that eConsent improves the consent process
  • 96% of patients prefer eConsent over paper
  • 66% of top 50 Pharma companies are engaged or planning an eConsent initiative in the near future

Source: 14 Drivers of eConsent Adoption in Clinical Trials


Become an eConsent Certified Professional

Attend our complimentary eConsent information session for research sites and become a Signant Health Certified eConsent Professional (ECP)- Level 1.

Let IRBs, Sponsors and your peers know you're the go to for eConsent insights by watching this session. 


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