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INSTITUTIONAL ETHICS REVIEW COMMITTEE CONTINUING REVIEW REPORT FORM Protocol No.: Institute/Department: Sponsor/CRO: Protocol Title: CT Phase/CT Type: Implementation Date: Continuing Review Date:
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How to fill out continuing review report form

01
To fill out the continuing review report form, follow these steps:
02
Start by providing the necessary identification information such as the title of the study, the investigator's name, and the IRB protocol number.
03
Describe any modifications made to the study since the last review, including changes to the study design, procedures, or informed consent process.
04
Provide a summary of the study's progress and the number of participants enrolled to date.
05
Assess and report any adverse events or unanticipated problems that have occurred during the study.
06
Review the study's data and determine if any changes are necessary to improve the study's design or conduct.
07
Discuss any challenges or issues faced during the study and how they were resolved.
08
Submit any additional documents or information required by the IRB for the review process.
09
Review the completed form for accuracy and completeness before submitting it for the continuing review process.

Who needs continuing review report form?

01
The continuing review report form is typically required by institutional review boards (IRBs) or ethics committees overseeing research studies involving human subjects.
02
Researchers conducting studies involving human subjects are the primary individuals who need to fill out this form as part of the ongoing review process.
03
It ensures that the study is still ethically sound and compliant with applicable regulations and guidelines.
04
In some cases, sponsors or funding agencies may also require the continuing review report form as part of their oversight and monitoring procedures.
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Continuing review report form is a document used to evaluate the progress of an ongoing research study and ensure compliance with regulatory requirements.
Principal investigators and research teams conducting research studies that involve human subjects are required to file continuing review report forms.
Continuing review report forms can be filled out online or on paper, following the specific instructions provided by the institution's Institutional Review Board (IRB).
The purpose of the continuing review report form is to assess the ongoing ethical and regulatory compliance of a research study involving human subjects.
Information such as any adverse events, changes to the study protocol, enrollment status, and any other updates related to the ongoing research study must be reported on the continuing review report form.
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