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CONTINUING REVIEW PROGRESS REPORT×PLEASE NOTE: If no Continuing Review Report is received, this protocol will expire and will be permanently closed at UMC. UMC IRB#: PRINCIPAL INVESTIGATOR: Protocol
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How to fill out continuing review progress report

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How to fill out continuing review progress report

01
To fill out a continuing review progress report, follow these steps:
02
Review the research protocol and familiarize yourself with the specific requirements for the progress report.
03
Gather all necessary information, such as participant enrollment numbers, adverse events, protocol deviations, and any updates to the research procedures or interventions.
04
Open the continuing review progress report form and start filling out the required sections.
05
Provide a summary of the progress made since the last review, including any significant findings or changes in the research.
06
Document participant enrollment numbers, retention rates, and any challenges faced in recruitment.
07
Describe any adverse events that occurred during the reporting period, noting the severity and the actions taken to address them.
08
Report any protocol deviations and explain how they were managed and minimized.
09
Include any updates or modifications to the research procedures or interventions, as well as the rationale behind them.
10
Discuss any changes to the risk-benefit ratio and the steps taken to ensure participant safety and welfare.
11
Provide a brief conclusion summarizing the overall progress and any future plans or actions required.
12
Review and proofread the progress report for accuracy and completeness.
13
Submit the completed continuing review progress report to the appropriate institutional review board (IRB) or ethics committee.
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Note: The specific format and requirements for the report may vary depending on the institution and the nature of the research.

Who needs continuing review progress report?

01
Continuing review progress reports are typically required by institutional review boards (IRBs) or ethics committees overseeing research studies involving human participants.
02
Researchers conducting clinical trials, observational studies, or other types of research involving human subjects may need to submit continuing review progress reports.
03
The need for a continuing review progress report may vary based on the duration of the study, the complexity of the research, and the regulations and policies of the institution or funding agencies involved.
04
It is important for researchers to consult the specific guidelines and requirements set forth by their IRB or ethics committee to determine if a continuing review progress report is needed for their study.

What is CONTINUING REVIEW PROGRESS REPORT Form?

The CONTINUING REVIEW PROGRESS REPORT is a Word document that should be submitted to the relevant address in order to provide some information. It has to be completed and signed, which can be done manually, or with a particular software like PDFfiller. It helps to complete any PDF or Word document directly in your browser, customize it depending on your needs and put a legally-binding e-signature. Once after completion, you can send the CONTINUING REVIEW PROGRESS REPORT to the appropriate individual, or multiple ones via email or fax. The editable template is printable as well due to PDFfiller feature and options offered for printing out adjustment. In both electronic and physical appearance, your form should have a clean and professional appearance. You may also save it as the template for further use, there's no need to create a new blank form again. You need just to customize the ready document.

Template CONTINUING REVIEW PROGRESS REPORT instructions

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CONTINUING REVIEW PROGRESS REPORT word template: frequently asked questions

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Continuing review progress report is a document that outlines the progress of a research study that has an ongoing review process to ensure compliance with regulations and protocols.
Researchers and institutions conducting the research study are required to file continuing review progress reports.
Continuing review progress reports can be filled out by providing updated information on the study protocol, any changes made, adverse events, and the status of the research study.
The purpose of the continuing review progress report is to ensure that the research study is being conducted in compliance with regulations and protocols, and that any changes are documented and reviewed by the appropriate authorities.
Information that must be reported on the continuing review progress report includes updated study protocol, any changes made, adverse events, and the status of the research study.
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