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.