Study Staff Orientation: Operationalizing Regulatory Compliance: The Informed Consent Process

This module will review the informed consent process in research, a critical component of our efforts to protect the rights, safety, and welfare of research subjects. Content includes a definition of informed consent; guidelines for developing the document, including writing for understanding; how to obtain and document consent; and special issues in informed consent.

Approximate time for completion: 25 minutes

Please register for this course using class code CTSIHU_SSO_InforConsent_eLearnView more information on how to register.


Wake Forest CTSI

Target Audience

Study Coordinators
Undergraduate and Post-Baccalaureate Students
Graduate Students

Delivery Method


RCR Credit

0.5 Credit(s)