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DocuSign Envelope ID: D75F42C759FE43A9987804031EB1E432990Form (Rev. January 2020)EXTENDED TO MAY 17, 2021, OMB No. 15450047Return of Organization Exempt From Income Tax2019Under section 501(c), 527,
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PDF informed consent is a document used to inform individuals about the risks, benefits, and procedures involved in a particular activity or research study, and to obtain their voluntary agreement to participate.
Researchers, healthcare providers, and organizations conducting activities or research studies that involve human subjects are required to file PDF informed consent forms.
PDF informed consent forms can be filled out by providing detailed information about the study or activity, the risks and benefits involved, and obtaining a signature from the participant indicating their voluntary agreement.
The purpose of PDF informed consent is to ensure that individuals are fully informed about the risks and benefits of participating in a study or activity, and to obtain their voluntary agreement to participate.
PDF informed consent forms must include information about the study or activity, the potential risks and benefits, the procedures involved, confidentiality measures, and the participant's rights.
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