Electronic Informed Consent (eIC): How The FDA/OHRP Final Guidance Affects You: January 29, 2019 Webinar

1/4/2019

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Topic: Electronic Informed Consent (eIC): How The FDA/OHRP Final Guidance Affects You

Date: January 29, 2019

Time: 1:00 p.m. – 2:30 p.m. EST

Duration: 90 minutes

Sponsored by: Life Science Training Institute

Webinar: Live interactive session. Recording will be available for 30 days.

Sign up here.

Description:

The US Food and Drug Administration (FDA) and Office for Human Research Protections (OHRP) finalized a guidance on electronic informed consent (eIC) that supports its use. eIC can support effective information delivery and improved comprehension. Following the guidance ensures proper oversight and adherence to the regulations while using eIC.

Join our own Sandra “SAM” Sather for this interactive training session on Electronic Informed Consent. Learn how the FDA / OHRP final guidance affects you.

Key take away benefits:

  • Learn about how eIC affects recruitment, compliance, and retention

  • Explore key activities for eIC integration

  • Discover how eIC impacts data protection and audit readiness

- The Clinical Pathways Team

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