Documenting Consent Electronically or for Remote Subjects Guidance

Information previously provided on this page has been relocated to our new IRB website.

Please visit the Consent Processes and Documentation section of the Investigator Manual for information about electronic and remote consent.

See Also:

• Use of Email for Research Purposes Guidance
• Initial Recruitment Contact and Screening Guidance
• Waiver of Signed Consent
• Guidance on FDA Regulation of Medical Mobile Apps