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Central Adelaide Local Health Network CAN Research ServicesParticipant Information Sheet/Consent Form Research Governance Review Guidelines Documents needed when submitting Picks for review: REC Approval
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How to fill out participant information sheetconsent form

01
Begin by providing the participant with the form to fill out.
02
Ensure that all sections of the form are completed accurately and legibly.
03
Clearly explain the purpose of the form and what information is being requested.
04
Have the participant sign and date the form to indicate their consent.
05
Collect the completed form and keep it in a safe and secure location.

Who needs participant information sheetconsent form?

01
Participant information sheet/consent form is needed for any individual participating in a research study, clinical trial, or any activity that requires informed consent.
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Participant information sheet/consent form is a document that provides information about a research study to potential participants and ensures that they understand the risks and benefits of participating.
Researchers conducting a study that involves human subjects are required to provide a participant information sheet/consent form to participants.
The participant information sheet/consent form should be filled out by the researcher conducting the study and should include information about the study purpose, risks, benefits, and participant rights.
The purpose of the participant information sheet/consent form is to ensure that participants are fully informed about the study and can make an informed decision about whether or not to participate.
The participant information sheet/consent form must include details about the study purpose, procedures, risks, benefits, confidentiality, and participant rights.
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