OVERVIEW
This Quickguide provides instructions for completing the Waiver of Consent (WoC) Application.
BEFORE YOU BEGIN
- Consider printing a copy of the Waiver of Consent Request Supplemental Form to use as reference as you complete the Application in IRBManager.
- Review the Determining Waiver of Consent Requirements Quickguide to determine if a waiver of consent is appropriate.
STEPS
INSTRUCTIONS
The investigator or designee answers all questions on the CIRB Waiver of Consent Application.
![Steps](/themes/custom/ncicirb/images/quickguides/ArrowBlack-01.jpg)
COMPLETE THE WAIVER OR ALTERATION OF REGULATORY ELEMENTS OF INFORMED CONSENT QUESTIONS
- Question 1: Select the type of waiver requested. For more information on this determination, refer to the Determining Waiver of Consent (Woc) Quickguide. If a waiver or alteration of the required elements of consent is requested, use the checkboxes to select the elements being waived or altered. Use the text box to provide a description of research activities and a rationale for waiving or altering the selected elements.
- Questions 2-6: These questions are used to document the regulatory criteria necessary for approval of a waiver or alteration of the elements of informed consent. Answer each question and use the text box to provide the details of research activities or rationale as requested.
![Steps](/themes/custom/ncicirb/images/quickguides/ArrowBlack-02.jpg)
COMPLETE WAIVER OF DOCUMENTATION OF INFORMED CONSENT QUESTIONS
- Questions 1-4: These questions are used to document the regulatory criteria necessary for approval of a waiver of documentation of consent. Answer each question and use the text box to provide the details of research activities or rationale as requested.