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INSTITUTIONAL REVIEW BOARD Consent Form Checklist The checklist provided below is presented as guidance for persons developing and reviewing applications to the CSU Institutional Review Board (IRB)
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How to fill out institutional review board consent
How to fill out institutional review board consent
01
Step 1: Start by obtaining the necessary documents for the Institutional Review Board (IRB) consent process, including the consent form and any supporting materials.
02
Step 2: Read and understand the purpose of the study and the specific requirements outlined by the IRB regarding consent.
03
Step 3: Prepare the consent form by providing all the required information, such as the study title, researcher's name, contact information, and study description.
04
Step 4: Clearly explain the purpose, procedures, and potential risks and benefits of participating in the study within the consent form.
05
Step 5: Include sections for participants to indicate their voluntary agreement to participate, their understanding of their rights, and their contact information.
06
Step 6: Ensure the language used in the consent form is clear, concise, and easily understandable by the target participants.
07
Step 7: Review the completed consent form for any errors, inconsistencies, or missing information before submission to the IRB.
08
Step 8: Submit the consent form and any supporting materials to the IRB for review and approval.
09
Step 9: Wait for the IRB's decision and follow any additional instructions or modifications requested.
10
Step 10: Once you receive IRB approval, distribute the consent form to potential participants, answer any questions they may have, and obtain their signed consent.
Who needs institutional review board consent?
01
Researchers conducting studies involving human subjects.
02
Academic institutions or organizations that oversee research involving human subjects.
03
Medical professionals and healthcare providers conducting research or clinical trials.
04
Pharmaceutical companies and drug manufacturers involved in human subject research.
05
Anyone involved in research studies that require compliance with ethical standards and protection of human subjects.
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