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North Texas Regional Institutional Review BoardContinuing Review Form Federal regulations require an Institutional Review Board (IRB) to conduct a Continuing Review of all research projects involving
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How to fill out continuing review of a

01
Start by reading the instructions provided by your institution or the organization responsible for the continuing review process.
02
Familiarize yourself with the purpose of the continuing review and the specific requirements for filling out the form.
03
Gather all the necessary information and documentation related to the research or study that requires continuing review.
04
Review the previous review documents, if applicable, to ensure consistency and address any changes or updates.
05
Begin the form by providing basic information such as the title of the study, the principal investigator's name, and contact details.
06
Proceed to answer each section or question on the form accurately and thoroughly.
07
Pay close attention to any specific guidelines or instructions provided for each section.
08
If there are any potential risks or changes related to the research, make sure to address them appropriately and provide any necessary justifications or modifications.
09
Include any additional documents or supporting materials required by the form or requested by the institution.
10
Once you have completed filling out the form, review it carefully to ensure accuracy and completeness.
11
Submit the completed continuing review form according to the designated submission process and timeline.
12
Keep a copy of the submitted form and any supporting documents for your records.
13
Monitor any communication or feedback from the reviewing committee or institution regarding the continuing review status or additional requirements.

Who needs continuing review of a?

01
Researchers or individuals involved in conducting research or studies that fall under the jurisdiction of an institutional review board (IRB) or similar ethics committee.
02
Institutions or organizations that require ongoing review of research protocols to ensure compliance with ethical standards and regulations.
03
These may include academic institutions, research hospitals, pharmaceutical companies, or any entity involved in research involving human subjects.

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Continuing review of a refers to the ongoing assessment of an ongoing research study by an Institutional Review Board (IRB) to ensure that the rights and welfare of participants are protected throughout the duration of the study.
Researchers or principal investigators conducting studies that involve human participants are typically required to file a continuing review with their Institutional Review Board (IRB).
To fill out a continuing review, researchers should provide updated information about the study's progress, any adverse events, changes in research protocol, and updated consent forms. Specific forms and requirements may vary by IRB.
The purpose of continuing review is to ensure ongoing oversight of the research to protect the rights and welfare of participants and to assess the ethical and scientific merit of the study as it progresses.
Information that must be reported typically includes enrollment numbers, any adverse events, changes to the study protocol, amendments to informed consent documents, and the overall status of the study.
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