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NH GRI IRB Checklist: Continuing Reviews or Terminations (Include 1 copy with submission) Principal Investigator: Protocol Number: Title: Check one: I. II. III. Subject accrual ongoing (Complete Section
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How to fill out nhgri irb checklist continuing:

01
Review the checklist guidelines provided by the National Human Genome Research Institute (NHGRI) to familiarize yourself with the required information and documentation.
02
Gather all necessary documents, such as research protocols, informed consent forms, recruitment materials, and data management plans.
03
Begin filling out the checklist by providing basic information about the research project, including the project title, principal investigator's name, and contact information.
04
Proceed to answer specific questions related to the research project, such as the study design, participant recruitment methods, data collection procedures, and potential risks and benefits for participants.
05
Evaluate whether the research involves vulnerable populations, such as children, pregnant women, or prisoners, and provide additional information as required.
06
Ensure that all ethical aspects are appropriately addressed, including obtaining informed consent, protecting participant privacy and confidentiality, and mitigating any potential conflicts of interest.
07
If applicable, describe any plans for data sharing, secondary use of data, or future collaborations.
08
Complete any additional sections, such as those related to human subjects training, institutional review board (IRB) approval status, and data safety monitoring.
09
Review the completed checklist to ensure accuracy and completeness.
10
Submit the checklist along with all required documentation to the designated NHGRI IRB or the corresponding institutional review board.

Who needs nhgri irb checklist continuing:

01
Researchers conducting human genomics or genetics research that falls under the purview of the NHGRI.
02
Institutions or organizations overseeing such research that require documentation and compliance with the NHGRI IRB checklist.
03
Ethical review boards, both internal and external, that evaluate and approve human research projects in line with NHGRI guidelines.
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The NHGRI IRB checklist continuing is a form used to ensure that ongoing research projects are being conducted in compliance with ethical guidelines and regulations.
Principal Investigators of research projects and their research teams are required to file the NHGRI IRB checklist continuing.
The NHGRI IRB checklist continuing can be filled out online or in hard copy, following the instructions provided by the NHGRI IRB office.
The purpose of the NHGRI IRB checklist continuing is to ensure that ongoing research projects are conducted ethically and in compliance with regulations.
Information such as any protocol deviations, adverse events, changes to the study protocol, and status updates on the research project must be reported on the NHGRI IRB checklist continuing.
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