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IRB NUMBER: 2030559 IRB APPROVAL DATE: 04/30/2020 IRB EXPIRATION DATE: 04/19/2021UNIVERSITY OF CALIFORNIA, SAN FRANCISCO Consents TO BE IN RESEARCH Study Title:Assessing the Safety of Pregnancy In
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How to fill out documentation of informed consent

01
Ensure that the participant fully understands the purpose of the study.
02
Provide all necessary information about the study procedures, risks, and benefits.
03
Clearly explain the participant's rights and the voluntary nature of participation.
04
Give the participant enough time to review the documentation and ask any questions.
05
Have the participant sign and date the informed consent form to indicate their agreement.

Who needs documentation of informed consent?

01
Anyone participating in a research study or clinical trial needs documentation of informed consent.
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The documentation of informed consent is a form signed by a patient or research subject that acknowledges their understanding of the risks and benefits of a medical procedure or research study.
Healthcare providers, researchers, or anyone conducting a medical procedure or research study is required to file documentation of informed consent.
Documentation of informed consent is typically filled out by providing information about the procedure or study, including risks and benefits, and obtaining the signature of the patient or research subject.
The purpose of documentation of informed consent is to ensure that individuals are fully informed about the risks and benefits of a medical procedure or research study before they agree to participate.
Documentation of informed consent must include information about the procedure or study, potential risks and benefits, confidentiality, and the right to withdraw from the study at any time.
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