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This document serves as an educational presentation on the submission process for new studies to the Institutional Review Board (IRB) at Tufts-New England Medical Center and Tufts University, defining
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How to fill out new study submissions to
How to fill out New Study Submissions to the IRB
01
Prepare your research protocol outlining the study objectives, methodology, and participant criteria.
02
Complete the IRB application form ensuring all required sections are filled out accurately.
03
Gather necessary supplementary documents such as informed consent forms, recruitment materials, and any survey instruments.
04
Provide detailed information about potential risks and benefits to participants.
05
Ensure that all investigators and key personnel are listed and their qualifications are documented.
06
Submit the application and accompanying materials through your institution’s IRB submission portal.
07
Review feedback from the IRB and make any necessary revisions to the submission.
08
Attend any required IRB meetings or discussions to answer questions regarding your submission.
Who needs New Study Submissions to the IRB?
01
Researchers conducting studies involving human subjects.
02
Students working on thesis or dissertation projects involving human subjects.
03
Institutions seeking to ensure compliance with ethical standards for research.
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What is New Study Submissions to the IRB?
New Study Submissions to the IRB are formal requests submitted to the Institutional Review Board (IRB) for approval of new research studies involving human subjects, ensuring that ethical standards are upheld.
Who is required to file New Study Submissions to the IRB?
Researchers and institutions that are planning to conduct studies involving human subjects are required to file New Study Submissions to the IRB.
How to fill out New Study Submissions to the IRB?
To fill out New Study Submissions to the IRB, researchers must complete the required forms by providing detailed information about the study's purpose, methodology, and potential risks, ensuring compliance with ethical standards.
What is the purpose of New Study Submissions to the IRB?
The purpose of New Study Submissions to the IRB is to protect the rights and welfare of human subjects involved in research and to ensure that all studies meet ethical and regulatory standards.
What information must be reported on New Study Submissions to the IRB?
New Study Submissions to the IRB must include information such as the study's title, objectives, participant criteria, methodologies, potential risks and benefits, consent processes, and funding sources.
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