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Register your Institutional Review Board (IRB) for human subject research at Icahn School of Medicine. Compliance with HHS and FDA regulations.
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The IRB registration form is a document used to register Institutional Review Boards (IRBs) with the appropriate regulatory bodies, ensuring that the board complies with federal regulations regarding human subjects research.
Institutions that conduct research involving human subjects and have an IRB are required to file the IRB registration form.
To fill out the IRB registration form, institutions must provide details such as the IRB's name, address, and the name of the institution, as well as information about the members of the IRB and their qualifications.
The purpose of the IRB registration form is to provide oversight and ensure that IRBs are meeting ethical and regulatory standards in the protection of human subjects in research.
The IRB registration form must report information including the IRB's name, contact information, member qualifications, and any relevant policies or procedures related to human subjects protection.
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