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CONTINUING REVIEW FORM for NUNS Institutional Review Board (IRB)Rev 07/19/16 skin accordance with Federal Regulations 45CFR46, the IRB must review nonexempt protocols at least annually, or more frequently
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How to fill out continuing review form for

How to fill out continuing review form for
01
Step 1: Start by reviewing your research protocol and any previous continuing review forms that you have filled out.
02
Step 2: Make sure you have all the necessary information and documentation for the review, such as any changes or updates to your research protocol, informed consent forms, and recruitment materials.
03
Step 3: Begin filling out the continuing review form by providing basic information about your study, such as the title and principal investigator's name.
04
Step 4: Answer any questions related to the progress of your study, such as recruitment updates, enrollment numbers, and any adverse events that have occurred since your last review.
05
Step 5: Provide any updates or changes to your study protocol, including modifications to the research design, interventions, or participant population.
06
Step 6: Upload any supporting documents or materials, such as updated informed consent forms or participant recruitment materials.
07
Step 7: Complete any required sections related to ethical considerations, such as providing information on any potential risks or benefits to participants.
08
Step 8: Review your completed continuing review form for any errors or missing information before submitting it for review.
09
Step 9: Submit the form to the appropriate review board or ethics committee for evaluation and approval.
10
Step 10: Follow up with any additional information or clarifications requested by the review board, and make any necessary revisions before final approval.
Who needs continuing review form for?
01
Researchers involved in human subjects research projects that are ongoing and require ongoing review and oversight by an Institutional Review Board (IRB) or ethics committee need to fill out continuing review forms.
02
Investigators who have obtained initial IRB approval for their research study are usually required to undergo periodic continuing review to ensure the safety and ethical conduct of the study.
03
Researchers who have made changes to their study protocol or have new information to report since their last review may also need to fill out continuing review forms to update the review board on these changes.
04
Continuing review forms are necessary for researchers who want to maintain compliance with ethical guidelines and regulations and ensure that their study continues to meet the necessary standards for human subjects research.
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What is continuing review form for?
The continuing review form is used to evaluate the ongoing progress of a research study and ensure that it is being conducted in accordance with ethical standards and regulatory requirements.
Who is required to file continuing review form for?
Principal investigators and study sponsors are required to file a continuing review form for any ongoing research studies that have received prior approval from an Institutional Review Board (IRB).
How to fill out continuing review form for?
To fill out a continuing review form, researchers should provide updates on the study's progress, any changes to the protocol, participant enrollment numbers, adverse events, and other relevant information that reflects the current status of the research.
What is the purpose of continuing review form for?
The purpose of the continuing review form is to ensure the ongoing protection of human subjects involved in research studies and to confirm that the research complies with ethical guidelines and regulatory requirements.
What information must be reported on continuing review form for?
The information that must be reported includes updates on participant enrollment, adverse events or side effects, any modifications to the research protocol, and findings related to the safety and efficacy of the study.
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