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CONSENT FOR MINIMAL RISK STUDIESTHAT ARE NOT CLINICAL TRIALS(ADMINISTRATIVE REVIEW)Revised 04/04/2023Minimal Risk to subjects means that the probability and magnitude of harm or discomfort anticipated
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How to fill out consent for minimal risk

01
Clearly explain the purpose and nature of the research.
02
Provide information about any potential risks or benefits to the participants.
03
Ensure that participants understand that participation is voluntary.
04
Obtain written consent from participants or their legal guardians if they are unable to give consent themselves.
05
Provide contact information for any questions or concerns about the study.

Who needs consent for minimal risk?

01
Researchers conducting studies that involve minimal risk to participants need to obtain consent from the participants.

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Consent for minimal risk is a form of permission obtained from participants in a research study where the risks are deemed minimal.
Researchers conducting studies that involve minimal risk to participants are required to file consent for minimal risk.
Consent for minimal risk should be filled out by providing clear and concise information about the study, risks involved, and the rights of participants.
The purpose of consent for minimal risk is to ensure that participants are fully informed about the study and voluntarily agree to participate.
Consent for minimal risk must include information about the study objectives, risks involved, procedures, benefits, confidentiality, and the rights of participants.
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