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Attestation Form Prepared in accordance with Section 15 of the Broader Public Sector Accountability Act, 2010 (BP SAA) To:The Board of Salt Area Hospital, (the Board)From: Ila Watson President and
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How to fill out research ethics board reb

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How to fill out research ethics board reb

01
Obtain the necessary forms and guidelines from the research ethics board (REB)
02
Fill out the required sections of the form, providing detailed information about the research study, including the purpose, methodology, risks, and benefits
03
Include information about how participants will be recruited, informed consent procedures, data collection and storage methods, and any potential conflicts of interest
04
Ensure all researchers involved in the study have completed any required ethics training and provide documentation of this with the application
05
Submit the completed application and any required supporting documents to the REB for review and approval
06
Address any feedback or revisions requested by the REB before final approval is granted

Who needs research ethics board reb?

01
Researchers conducting studies involving human participants
02
Institutions or organizations conducting research that involves human subjects
03
Any individual or group seeking to ensure that their research meets ethical guidelines and standards
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The Research Ethics Board (REB) is a group responsible for reviewing research proposals to ensure they meet ethical standards.
Researchers conducting studies involving human subjects are required to file with the Research Ethics Board (REB).
To fill out a Research Ethics Board (REB) form, researchers must provide detailed information about their study protocol, risks and benefits, and how participant confidentiality will be maintained.
The purpose of the Research Ethics Board (REB) is to protect the rights and well-being of research participants by ensuring that research studies are conducted ethically.
Researchers must report details about their study protocol, potential risks and benefits to participants, the informed consent process, and how participant confidentiality will be maintained.
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