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Get Application For Approval For Human Subjects Research Request For ...
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How to fill out the application for approval for human subjects research request for exemption online
Filling out the application for approval for human subjects research is an essential step for any researcher engaging in studies involving human participants. This guide aims to provide clear and supportive instructions for completing the form online, ensuring a smooth process for both experienced and novice users.
Follow the steps to complete the application form effectively.
- Press the ‘Get Form’ button to acquire the form and open it in your preferred editor.
- Begin with the project title: Enter a concise and descriptive title for your research project in the designated area.
- List the principal investigator(s): Enter the name, department, and email address of each principal investigator, ensuring correct spelling and departmental affiliation.
- If applicable, include the faculty supervisor's details: Only provide this information if the principal investigator is a student. Include the name, department, and email address.
- Indicate funding source: If the project is funded, specify the name of the agency or source, and the title and contract number of the grant if available.
- Specify the dates of the study: Clearly outline the start and end dates for the research project.
- Select the exemption category: Reference the exemption categories outlined in the guide and cite the relevant paragraph(s) that apply to your research.
- Signatures: Ensure that the principal investigator(s) and faculty supervisor (if applicable) sign and date the form to validate the application.
- Review and approval: After submission, await review and approval from the institutional review board liaison, who will also sign the form.
- Final steps: After processing, you may save your changes, download, print, or share the completed form as needed.
Complete your application online today to facilitate your research project!
The regulations do outline the criteria for IRB approval of research. 21 CFR 56.111(a)(1) requires the IRB to assure that risks to the subjects are minimized. 21 CFR 56.111(a)(2) requires the IRB to assure that the risks to subjects are reasonable in relation to the anticipated benefits.
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