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NorthwellHealthHumanResearchProtectionProgram ResearchComplianceGCP/ISODeviceStudyReviewChecklist The Human Research Protection Program at Northwell Health conducts routine and for cause reviews of
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Begin by carefully reading the instructions provided on the form. Understand the purpose and requirements of the form to ensure accurate completion.
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Provide your personal information accurately. This may include your name, contact details, and any relevant identification numbers.
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Clearly state the purpose of the research and provide a brief overview of the study. This section helps the reviewing authorities understand the context and significance of the research.
04
Explain the methodology and procedures that will be employed during the research. Detail the steps involved, including any potential risks or benefits for the participants.
05
If applicable, address the ethical considerations involved in the research. Describe how participant confidentiality and privacy will be protected, and explain any measures taken for obtaining informed consent.
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Include any necessary supporting documents, such as consent forms, questionnaires, or survey instruments, that are relevant to the research.
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Provide a timeline outlining the duration of the study and key milestones. This helps the reviewing authorities understand the expected timeframe for completion.
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List any financial support or funding sources associated with the research project. This includes any grants, sponsorships, or resources that are received for conducting the study.
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Once the form is completed, review it thoroughly to ensure all necessary information is included and accurately presented. Make any necessary corrections or additions.
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Finally, submit the completed form along with any required attachments to the appropriate research ethics or institutional review board for review and approval.

Who needs form human research protection?

The form for human research protection is typically required by researchers or institutions conducting studies involving human subjects. This includes academic researchers, scientists, medical professionals, and other individuals involved in conducting research within the fields of psychology, medicine, sociology, and other related disciplines. The form ensures that ethical considerations and participant protections are in place before any research involving human subjects can proceed.
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Form human research protection is a document used to ensure that research involving human subjects is conducted ethically and in compliance with regulations.
Researchers conducting studies involving human subjects are required to file form human research protection.
Form human research protection should be filled out by providing detailed information about the research study, the procedures involved, and the measures taken to protect the rights and safety of human subjects.
The purpose of form human research protection is to ensure that research involving human subjects is conducted in an ethical and responsible manner.
Form human research protection typically requires information about the study design, risks and benefits to participants, informed consent procedures, and how confidentiality will be maintained.
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