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Office of Research and Sponsored Programs Sam Houston State University 903 Bowers Blvd, PO Box 2448 Huntsville, TX 77341 Phone: 936.294.3621 Fax: 936.294.3622 Continuing Review Form I. Protocol Information
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How to fill out continuing review original
How to Fill Out Continuing Review Original:
01
Start by reviewing the previous version of the review to familiarize yourself with any changes or updates that need to be made.
02
Carefully read through the instructions provided on the continuing review form to understand the specific information and documentation required.
03
Begin by filling out the basic information section, which usually includes your name, contact information, and the name of the study or project.
04
Provide a detailed description of the study or project, including its objectives, methodology, and any potential risks or benefits for participants.
05
Indicate whether any amendments have been made to the study since the last review, and if so, describe the changes that have been implemented.
06
Explain any deviations from the initial study protocol, if applicable, and provide a rationale for these modifications.
07
Evaluate the overall progress of the study, including recruitment of participants, data collection and analysis, and any challenges or issues encountered.
08
Describe any adverse events or unanticipated problems that have occurred during the course of the study. Include information on how these were managed and the steps taken to prevent recurrence.
09
Provide information on any changes to the research team, such as new members joining or existing members leaving the study.
10
Remember to sign and date the review form, and submit it within the specified timeline.
Who Needs Continuing Review Original:
01
Researchers conducting studies or projects that involve human participants.
02
Institutional review boards (IRBs) or research ethics committees responsible for reviewing and approving research involving human subjects.
03
Sponsor organizations funding or overseeing the research, ensuring compliance with ethical guidelines and regulatory requirements.
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What is continuing review original?
Continuing review original is a process by which Institutional Review Boards (IRBs) reevaluate research protocols at regular intervals to ensure the continued protection of human subjects.
Who is required to file continuing review original?
Researchers conducting human subjects research are typically required to file continuing review original with the IRB.
How to fill out continuing review original?
Continuing review original typically involves submitting updates on the progress of the research, any adverse events, changes to the protocol, and any new information that may impact the ethical considerations of the study.
What is the purpose of continuing review original?
The purpose of continuing review original is to ensure that human subjects are protected throughout the duration of the research study.
What information must be reported on continuing review original?
Information such as any changes to the research protocol, adverse events, updates on the progress of the study, and any new information that may impact the ethical considerations of the study must be reported on continuing review original.
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