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Use for both continuing review and as a final report to close a HUD Use. If modifications are being requested, submit a separate request for a modification. Protocol Name:Physician:Primary Contact:Enrollment
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How to fill out form continuing review progress

01
To fill out the form continuing review progress, follow these steps:
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Begin by opening the form on your computer or printing a hard copy if preferred.
03
Start by providing the required information at the top of the form, such as the study title, study ID, and principal investigator's name.
04
Next, review the progress of the study and provide an update in the designated section. This can include details on participant enrollment, any adverse events, protocol deviations, and any other relevant information.
05
If there are any changes to the study protocol or consent documents, be sure to include those updates in the appropriate section.
06
Ensure that any required signatures and dates are included where necessary.
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Finally, review the completed form for accuracy and completeness before submitting it to the appropriate review board or authority.

Who needs form continuing review progress?

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Form continuing review progress is typically needed by researchers, principal investigators, and individuals responsible for conducting and overseeing ongoing research studies.
02
It may also be required by the institutional review board (IRB) or ethics committee overseeing the study to ensure compliance with regulations and ethical standards.

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Form continuing review progress is a document used to assess and report the status of ongoing research projects that require periodic review by an institutional review board (IRB) to ensure compliance with ethical standards.
Researchers or principal investigators conducting studies involving human subjects that require IRB oversight are required to file the form continuing review progress.
To fill out the form continuing review progress, researchers should provide detailed updates regarding the study's status, including participant enrollment figures, any adverse events, changes to the study protocol, and plans for the continuation of the research.
The purpose of the form continuing review progress is to ensure that ongoing research remains ethical, complies with regulatory requirements, and protects the rights and welfare of participants.
Information that must be reported includes recruitment status, participant demographics, any incidents or adverse events, amendments to the study protocol, and future plans for the study.
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