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Submission#: 40973 IORG0000196 BORG#: U of Pittsburgh Institution: OMB No. 09900279 Approved for use through August 31, 2015, U.S. Department of Health and Human Services (HHS) Registration of an
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How to fill out irb pitt

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How to fill out IRB Pitt:

01
Start by visiting the official website of the University of Pittsburgh's Institutional Review Board (IRB) or navigate directly to the IRB Pitt page.
02
Familiarize yourself with the purpose and guidelines of the IRB Pitt, ensuring you understand the ethical considerations and regulatory requirements for conducting research involving human subjects.
03
Identify the specific forms or applications required for your research study. The IRB Pitt website should have a range of downloadable documents that correspond to different types of research protocols.
04
Carefully review the instructions for each form or application to understand the information needed and any supporting documents required.
05
Complete the necessary sections of the forms or applications, providing accurate and detailed responses to the questions asked. Make sure to include all required information such as study title, objectives, participant recruitment methods, data collection procedures, and potential risks and benefits.
06
If applicable, include any additional documents or materials requested by the IRB Pitt, such as consent forms, questionnaires, or study protocols. Ensure these documents comply with the IRB's formatting and content guidelines.
07
Double-check your completed forms for any errors or omissions before saving or printing them.
08
Prepare any supporting materials in the required format, such as electronic files, physical copies, or online links.
09
Submit your completed forms, applications, and supporting documents to the IRB Pitt. The submission process may vary, so carefully follow the outlined instructions on the website.
10
After submitting your materials, allow time for the IRB Pitt to review your research proposal. They may contact you for additional information or clarification if needed.
11
Once your research study is approved, ensure that you adhere to the conditions and reporting requirements outlined by the IRB Pitt throughout the duration of your study.
12
If any modifications to your research study are required or if you encounter any issues or concerns, promptly communicate with the IRB Pitt to seek guidance and resolution.

Who needs IRB Pitt:

01
Researchers or individuals planning to conduct research involving human subjects affiliated with the University of Pittsburgh or collaborating with Pitt researchers.
02
Students, faculty, or staff members who are undertaking research activities that involve human participants.
03
Anyone involved in projects that may require ethical review and approval to ensure the protection of human subjects and compliance with federal regulations.
Please note that the process of filling out IRB Pitt forms and the requirement for IRB approval may vary depending on the nature and scope of the research study. It is important to consult the IRB Pitt website, guidelines, and experts for accurate and up-to-date information specific to your research project.
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IRB PITT stands for Institutional Review Board at the University of Pittsburgh. It is a committee that reviews and approves research involving human participants.
Researchers and institutions conducting research involving human participants are required to file IRB PITT.
To fill out IRB PITT, researchers need to submit an application including information on the research protocol, risks and benefits to participants, and informed consent procedures.
The purpose of IRB PITT is to ensure the protection of human participants involved in research studies.
Researchers must report details of the research protocol, risks and benefits to participants, and informed consent procedures on IRB PITT.
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