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Humanitarian Use Device Progress Report Florida Hospital Tampa Bay Division IRB Continuing Review / Final Reportedly Board Continuing Review Instructions:Expedited Continuing Review Instructions: Submission
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How to fill out continuing review final report

01
To fill out the continuing review final report:
02
Gather all necessary documents and information related to the research project.
03
Start by providing the project title and the name of the principal investigator.
04
Include a summary of the research objectives and methods employed.
05
Summarize the findings or progress made so far.
06
Assess any potential risks or adverse events encountered during the research.
07
Provide any changes or modifications made to the research protocol.
08
Include a statement on whether the research is still in line with the original goals and objectives.
09
Mention any ethical considerations or issues brought up during the study.
10
Submit the report with all required signatures and supporting documents.
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Review the completed report for accuracy and completeness before submission.

Who needs continuing review final report?

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The continuing review final report is required for researchers and institutions conducting human subjects research that falls under the purview of an institutional review board (IRB). It is a regulatory requirement and ensures that the research project is being conducted ethically and in compliance with relevant regulations and guidelines.

What is Continuing Review / Final Report Form?

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Instructions for the Continuing Review / Final Report form

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The continuing review final report is a document that outlines the ongoing progress and status of a research study or project.
Researchers and principal investigators are typically required to file the continuing review final report.
The continuing review final report can typically be filled out online through the institution's research compliance system.
The purpose of the continuing review final report is to ensure that research studies are progressing as planned and in compliance with regulations and ethical standards.
The information that must be reported on the continuing review final report includes any updated study procedures, consent forms, adverse events, and any deviations from the original protocol.
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