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Continuing Review FormDear Principal Investigator(s):Federal regulations require that research protocols previously reviewed by the IRB submit a report annually if the research project is continues
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How to fill out continuing reviewhuman research protection

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How to fill out continuing reviewhuman research protection

01
Review the protocol and any changes made since the last review.
02
Complete the appropriate forms or documentation required by the institutional review board (IRB).
03
Provide any requested information or documentation to the IRB in a timely manner.
04
Ensure that all research team members are up to date on the protocol and any changes.
05
Obtain approval from the IRB before continuing with the research.

Who needs continuing reviewhuman research protection?

01
Researchers conducting human subjects research that has been approved by an institutional review board.

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Continuing review human research protection refers to the periodic assessment of ongoing research studies to ensure that they continue to meet ethical standards and comply with regulatory requirements for the protection of human subjects.
Researchers, institutions, and the Institutional Review Boards (IRBs) involved in human subjects research are required to file continuing reviews to ensure ongoing compliance with ethical and regulatory standards.
To fill out a continuing review for human research protection, researchers need to complete a designated form provided by their IRB, detailing the study's progress, any adverse events, changes to the protocol, and information on subject recruitment and retention.
The purpose of continuing review is to ensure that the research continues to be ethically conducted and that risks to participants remain minimized while benefits are maximized throughout the duration of the study.
Investigators must report information including the number of enrolled subjects, any adverse events or unanticipated problems, any changes to the study protocol, and updates on participant recruitment and retention.
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