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University of the District of Columbia Institutional Review BoardContinuing Review Application for Research Involving Human Participants IRB No. Date Received: Instructions to applicant for renewal:1.
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How to fill out continuing review application for

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How to fill out continuing review application for

01
Log in to the appropriate research application system.
02
Navigate to the section for continuing review applications.
03
Select the specific study for which you need to complete the continuing review application.
04
Carefully read the instructions and guidelines provided on the application form.
05
Begin filling out the required fields by providing accurate and up-to-date information.
06
Pay special attention to any sections requiring updates or changes from the previous review.
07
Complete any additional questions or sections as applicable to your specific study.
08
Review the filled-out application form for any errors or missing information.
09
Submit the completed continuing review application.
10
Monitor the status of your application through the research application system and follow up accordingly.

Who needs continuing review application for?

01
Continuing review application is required for researchers who are conducting studies that involve human subjects and have obtained initial approval from an Institutional Review Board (IRB). This application is necessary to ensure ongoing compliance with ethical guidelines and to review any changes or updates to the study protocol, participant consent forms, or other relevant study documents.

What is Continuing Review Application for Research Involving Human Participants Form?

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Instructions for the form Continuing Review Application for Research Involving Human Participants

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A continuing review application is for evaluating ongoing research studies to ensure they continue to meet ethical standards and regulatory requirements.
Researchers conducting human subjects research that requires periodic review to ensure the protection of participants.
The application typically involves completing a form that includes information on the study's progress, any changes to the protocol, and updates on participant safety.
The purpose is to assess the ongoing ethical and scientific validity of the research study and to protect the welfare of participants.
Information on participant enrollment, adverse events, changes to the study, and any new information that could affect the risk/benefit analysis.
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