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Participant Information Sheet/Consent Form Nonintervention Study Adult providing own consent Title Short Title Protocol Number Project Sponsor Coordinating Principal InvestigatorATHENA COVID-19 Genomics COVIDOZGenetics 2020001490 University
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01
Ensure all necessary fields on the participant information sheet/consent form are clearly labeled.
02
Provide clear instructions on how to fill out each section.
03
Make sure participants sign and date the form at the designated spaces.
04
Explain the purpose of each section and the importance of providing accurate information.
05
Have a designated person available to answer any questions or provide assistance if needed.

Who needs participant information sheetconsent form?

01
Researchers conducting studies that involve human participants.
02
Institutional review boards or ethics committees overseeing research studies.
03
Participants in the study who need to provide consent for their participation.
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The participant information sheet/consent form is a document that provides information to potential participants about the research study and obtains their consent to participate.
Researchers conducting a study involving human subjects are required to provide participants with a participant information sheet/consent form.
The participant information sheet/consent form should be filled out by the researcher with detailed information about the study, risks, benefits, and participant rights. It should also include a section for the participant to indicate their consent to participate.
The purpose of the participant information sheet/consent form is to ensure that participants are fully informed about the research study, their rights, and to obtain their voluntary consent to participate.
The participant information sheet/consent form must include details about the study purpose, procedures, risks, benefits, confidentiality, data management, and contact information for questions or concerns.
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