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This form is used to apply for expedited review of research activities involving human subjects that present minimal risk. It outlines eligibility criteria, responsibilities of the principal investigator,
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How to fill out expedited review of research

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How to fill out expedited review of research

01
Determine if your research qualifies for expedited review according to regulatory guidelines.
02
Complete the expedited review application form, ensuring all sections are filled out accurately.
03
Attach a detailed description of the research project, including objectives, methodology, and potential risks.
04
Include any relevant supporting documents, such as recruitment materials or consent forms.
05
Submit the completed application and documents to the appropriate review board or committee.
06
Await feedback or approval from the review board.

Who needs expedited review of research?

01
Researchers conducting minimal risk studies involving human subjects.
02
Investigators working on projects that involve previously collected data or non-invasive procedures.
03
Those seeking expedited review for projects related to urgent public health needs or disasters.
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Expedited review of research is a process that allows for a faster evaluation of specific types of research proposals that involve minimal risk to participants, as determined by an institutional review board (IRB).
Researchers conducting studies that involve minimal risk to participants and meet specific criteria set by the IRB are typically required to file for expedited review.
To fill out an expedited review application, researchers must complete the required forms provided by their IRB, detailing the study's purpose, methods, participant recruitment strategies, and potential risks.
The purpose of expedited review is to streamline the process for research projects that pose minimal risk, allowing them to be reviewed more quickly while still ensuring participant protections.
Researchers must report details such as the study's objectives, methodology, participant demographics, informed consent processes, risk assessment, and any relevant safety measures.
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