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Title: Obtaining Informed Consent from Research Subjects SOP Number: 1101Effective Date: June 2, 2017Previous Version Dates:1PurposeNo investigator conducting research under the auspices of the University
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How to fill out obtaining informed consent from

01
To fill out obtaining informed consent form, follow these steps:
02
Start by explaining the purpose and nature of the study or procedure to the participant.
03
Provide a clear description of the risks and benefits associated with the study or procedure.
04
Make sure to explain any alternative treatments or procedures that may be available.
05
Present the participant with a consent form that includes all the necessary information.
06
Ensure that the participant understands the content of the form and addresses any questions or concerns they may have.
07
Allow the participant enough time to carefully read and review the form.
08
Once the participant feels comfortable and fully informed, ask them to sign the consent form.
09
Make a copy of the signed form for both the participant and the researcher's records.
10
Keep the signed consent form in a safe and confidential manner for future reference.

Who needs obtaining informed consent from?

01
Obtaining informed consent is necessary for any research study or medical procedure that involves human participants.
02
This includes clinical trials, surveys, interviews, experiments, and any other form of study where data is collected from individuals.
03
Informed consent is a crucial ethical and legal requirement to ensure that participants are fully aware of the risks and benefits involved and have the opportunity to make an informed decision about their participation.
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Obtaining informed consent is the process of getting permission from an individual before conducting a specific activity or research.
Anyone who is conducting a research or activity that involves human subjects is required to obtain informed consent from the participants.
Informed consent forms should include details about the research or activity, potential risks and benefits, confidentiality, voluntary participation, and contact information.
The purpose of obtaining informed consent is to ensure that participants are fully informed about the research or activity they are participating in and voluntarily agree to take part.
Information that must be reported on obtaining informed consent forms includes details about the research or activity, potential risks and benefits, confidentiality, voluntary participation, and contact information.
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