Remote Informed Consent: The Same, but Different, but Still the Same

Presents remote consent considerations and scenarios.

Questions? Contact Us
Scroll Down Arrow

About this Webinar

With the transition to remote work due to the COVID-19 pandemic, research teams, Institutional Review Boards (IRBs), and others supporting human research have worked to develop alternate workflows for processes that would normally be done face-to-face.

This webinar explores the conduct of remote informed consent including components, process options, documentation requirements, and agency-specific regulatory requirements and flexibilities. The webinar discusses how to adapt face-to-face processes to remote, including options for electronic consent documentation. It includes real world examples in various research scenarios.

Webinar Demo:

Release Date: March 25, 2021

Language Availability: English

Suggested Audiences: Clinical Research Coordinators (CRCs), Faculty, Graduate Students, Investigators, IRB Administrators, IRB Members, Researchers, Students

Organizational Subscription Price: $300 per year/per site or included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person

Webinar Content

Remote Informed Consent: The Same, but Different, but Still the Same

Presented by: Belinda Smith, MS, RD, CCRC – University of Kentucky

Learning Objectives:

  • Consider requirements that apply to remote consent processes and documentation including HHS, HIPAA, and FDA regulated research.
  • Adapt informed consent components for a remote process including areas of regulatory flexibility afforded by agencies due to the pandemic.
  • Explore electronic consent solutions and challenges.
  • Review remote consent process examples in various research scenarios.

Recommended Use: Required
ID (Language): 20397 (English)

Learn More

Your Name(Required)
I'd Like To Receive Emails From CITI Program
This field is for validation purposes and should be left unchanged.