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TEMPLATE NONPARTICIPANT INFORMATION SHEET AND CONSENT FORM Please remove this text box when finalizing the documentGUIDELINES: With effect from 1 March 2023, all new IRB applications (for research
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Who needs cirb participant information sheet?

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What is CIRB Participant Ination Sheet and Consent ... Form?

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The CIRB Participant Information Sheet is a document that collects essential information regarding participants in a Clinical Investigation Research Board (CIRB) study.
Researchers and institutions conducting studies that fall under the jurisdiction of the CIRB are required to file the CIRB Participant Information Sheet.
To fill out the CIRB Participant Information Sheet, one must accurately provide details such as study title, participant demographics, consent information, and any relevant study protocols.
The purpose of the CIRB Participant Information Sheet is to ensure that researchers adhere to ethical standards by collecting necessary information regarding participant consent and details of the study.
Information such as participant identification, contact information, informed consent status, study location, and details of the research study must be reported on the CIRB Participant Information Sheet.
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