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This form is used to request a continuation of an approved research project beyond the one-year IRB approval period. The application must be submitted 30 days prior to the expiration of approval, including necessary modifications or changes to the research protocol.
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How to fill out continuing review of approved

01
Gather all necessary documents related to the approved study.
02
Review the original research protocol and any amendments that have been made.
03
Compile data on recruitment and enrollment status of participants.
04
Summarize any adverse events or unanticipated problems that occurred during the study.
05
Assess the progress of the study against the approved timeline and milestones.
06
Complete the continuing review application form, ensuring all sections are filled out accurately.
07
Attach any required supporting documents, such as updated consent forms or data analysis summaries.
08
Submit the completed application and documentation to the Institutional Review Board (IRB) before the expiration date.

Who needs continuing review of approved?

01
Researchers conducting ongoing studies that have been approved by the IRB.
02
Individuals or organizations that receive funding for research requiring ethical oversight.
03
Institutional Review Boards (IRBs) for monitoring study compliance and subject safety.

What is Continuing Review of Approved Research Form?

The Continuing Review of Approved Research is a Word document which can be completed and signed for specified purposes. Next, it is furnished to the exact addressee in order to provide some details of certain kinds. The completion and signing may be done in hard copy by hand or via an appropriate tool e. g. PDFfiller. These applications help to fill out any PDF or Word file without printing out. While doing that, you can customize its appearance depending on your requirements and put a valid digital signature. Once you're good, the user sends the Continuing Review of Approved Research to the recipient or several ones by email or fax. PDFfiller offers a feature and options that make your document of MS Word extension printable. It offers different settings when printing out. It doesn't matter how you distribute a form after filling it out - in hard copy or by email - it will always look professional and firm. In order not to create a new editable template from scratch over and over, make the original Word file into a template. Later, you will have an editable sample.

Instructions for the Continuing Review of Approved Research form

Before starting to fill out Continuing Review of Approved Research MS Word form, be sure that you prepared enough of necessary information. This is a important part, because typos can trigger unpleasant consequences beginning from re-submission of the whole entire blank and completing with missing deadlines and you might be charged a penalty fee. You need to be really careful filling out the digits. At first sight, it might seem to be quite simple. But nevertheless, it's easy to make a mistake. Some people use such lifehack as storing their records in another file or a record book and then attach it into documents' temlates. However, put your best with all efforts and present accurate and correct info in your Continuing Review of Approved Research word template, and doublecheck it while filling out the required fields. If it appears that some mistakes still persist, you can easily make corrections when working with PDFfiller tool without missing deadlines.

Frequently asked questions about the form Continuing Review of Approved Research

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Continuing review of approved refers to the ongoing evaluation of research studies that have already been approved by an institutional review board (IRB) to ensure they continue to meet ethical standards and regulatory compliance.
The principal investigator (PI) or the research team are typically required to file continuing reviews for any research studies that involve human subjects.
To fill out a continuing review, the investigator must complete the necessary forms provided by the IRB, summarizing the progress of the research, discussing any changes to the protocol, and reporting any adverse events.
The purpose of continuing review is to monitor the study's compliance with ethical standards and ensure the protection of participants, allowing IRBs to identify any potential issues that arise during the research process.
Information that must be reported includes recruitment and enrollment progress, any changes to the research protocol, results of the study so far, and any adverse events that have occurred.
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