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IRB Approved Document Release Date: 12/27/20179799FRED HUTCHINSON CANCER RESEARCH CENTER UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE Current version: 3 Previous version:2Management of Venous Thromboembolic
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To fill out a continuing review, follow these steps:
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Review the previous submission: Start by reviewing the information from the initial submission for the study.
03
Capture changes: Identify any changes made to the study design, procedures, or personnel since the last submission.
04
Update study information: Make sure to update any relevant study details such as the title, objectives, or funding sources.
05
Summarize study progress: Provide a summary of the progress made in the study since the last review.
06
Assess risks and benefits: Consider any new risks or benefits that have emerged during the study period.
07
Address ethical considerations: Discuss how the study continues to uphold ethical standards and protects the rights of participants.
08
Submit updated documents: Attach any updated documents or protocols to support the continuing review.
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Submit the review: Finally, submit the completed continuing review form for evaluation and approval.

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Continuing review is needed for researchers who are conducting human subject research.
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It is especially important in studies that involve ongoing data collection, interventions, or interactions with participants.
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Additionally, researchers who receive external funding or are affiliated with institutions that require continuing review should comply with this process.
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Continuing review - fred is a process by which the IRB evaluates the progress of an ongoing research study to ensure the protection of human subjects.
The principal investigator of the research study is required to file the continuing review - fred.
The continuing review - fred form can be filled out online or submitted to the IRB office via email or mail.
The purpose of continuing review - fred is to ensure that the research study is still in compliance with ethical standards and regulatory requirements.
The continuing review - fred must include updates on any changes to the study protocol, informed consent documents, or adverse events.
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