eConsent

Also known as
Also known as: 
  • Electronic Consent

Consenting participants to a prospective interventional/observational study can be an involved process. Keeping track of paper consent leads to extensive organizational and administrative overhead, and the use of electronic consent mechanisms can simplify this process, allowing study teams to streamline workflows and enhance regulatory compliance. 

To learn more about how to use eConsent for your research, contact econsent-support@med.cornell.edu  

Frequently Asked Questions

How does eConsent work?

What eConsent options are available?

How can I use eConsent?

Status

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