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[Insert Department][CONSENT/PARTICIPANT INFORMATION] Form [Insert Title of Study]Note to investigators: this template encompasses all of the required and some additional elements of informed consent,
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How to fill out sbe-sample-consent-short-form-exemptdocx

01
Open the 'sbe-sample-consent-short-form-exempt.docx' document on your computer.
02
Read the introductory information to understand the purpose of the consent form.
03
Fill in the participant's name and contact information in the designated fields.
04
Provide a brief description of the research study in the appropriate section.
05
Clearly outline the purpose of the study and what participation involves.
06
Specify any risks, benefits, and alternatives to participation.
07
Include information regarding confidentiality and how data will be handled.
08
Ensure that the participant understands that participation is voluntary.
09
Include space for the participant's signature and date.
10
Save the completed form and ensure a copy is provided to the participant.

Who needs sbe-sample-consent-short-form-exemptdocx?

01
Researchers conducting studies that require participant consent.
02
Institutional Review Boards (IRBs) needing to review consent processes.
03
Participants involved in research studies that require informed consent.

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sbe-sample-consent-short-form-exemptdocx is a template document designed to obtain consent from participants involved in research studies that are exempt from certain regulatory requirements.
Researchers and organizations conducting studies that involve human subjects and qualify for exemption from full IRB review are required to file this document.
To fill out the form, provide details about the study, participant rights, procedures, risks, benefits, and the investigator's information in the designated fields.
The purpose is to inform participants about the study, ensure they understand their role, and obtain their voluntary consent before participation.
Required information includes study title, purpose, procedures involved, potential risks, benefits, confidentiality assurances, and contact information for the research team.
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