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BACKGROUND In order to comply with Connecticut General Statutes 19a25 and Regulations of Connecticut State Agencies 19a251 through 19a254, the Connecticut Department of Public Health Human Investigations
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How to fill out continuing review of research

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How to fill out continuing review of research

01
Review the protocol of the research project
02
Update any changes or progress made in the research
03
Address any concerns or issues raised during the previous review
04
Submit the continuing review form and any required documentation to the appropriate institutional review board (IRB) or research ethics committee

Who needs continuing review of research?

01
Researchers conducting human subjects research
02
Institutions with an IRB or research ethics committee overseeing research projects

What is Continuing Review of Research / Study Closure Form?

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Continuing review of research is the ongoing evaluation of research projects by an Institutional Review Board (IRB) to ensure the protection of human subjects. It assesses the continued validity of the research, adherence to ethical guidelines, and any changes in risk associated with the research.
Researchers conducting studies that involve human subjects are required to file for continuing review, particularly if their research is subject to regulation by institutional or federal guidelines. This typically includes investigators receiving funding or conducting research that needs IRB oversight.
To fill out the continuing review of research, researchers must complete a designated form provided by their IRB. This typically includes updates on the progress of the study, any new findings, changes to the research protocol, and any adverse events that have occurred since the last review.
The purpose of continuing review of research is to ensure the ongoing safety and welfare of participants, confirm that the research follows ethical standards, and assess if the risks and benefits of the study remain appropriate over time.
Research investigators must report information including the number of participants enrolled, any adverse events, changes in study protocol, updated consent forms, and any new relevant literature that may impact the study.
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