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IRB Coordination across Passé Universities Preface University Institutional Review Boards (IRS) have jurisdiction to review all research (as defined in 45 CFR Part 46) that occurs on or uses human
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How to fill out irb coordination across passhe:

01
Start by familiarizing yourself with the IRB (Institutional Review Board) coordination process across the Pennsylvania State System of Higher Education (PASSHE). This process ensures that research involving human participants adheres to ethical guidelines.
02
Obtain the necessary documentation and forms required for the IRB coordination. These may include the application form, consent forms, and any supporting materials required for your research project.
03
Read and understand the guidelines provided by the IRB coordination across PASSHE. This will help you ensure that your research project aligns with the necessary ethical considerations and procedures.
04
Complete the application form accurately, providing all the required information about your research project. This includes details about the research design, methods, sample size, and any potential risks or benefits to the participants.
05
Prepare the consent forms that participants will need to sign before participating in your research. These forms should clearly outline the purpose of the study, any potential risks or benefits, and how their data will be handled and protected.
06
Submit your completed application and accompanying documents to the designated contact or office responsible for IRB coordination across PASSHE. Be sure to adhere to any deadlines and follow the submission instructions provided.
07
Wait for the IRB review process to be completed. This typically involves a thorough examination of your research proposal to ensure it meets ethical standards and protects the rights and welfare of the participants.
08
Address any feedback or modifications requested by the IRB during the review process. This may involve revising your research design, consent forms, or addressing any ethical concerns raised by the IRB.
09
Upon approval from the IRB, you can proceed with your research project. Ensure that you adhere to any stipulations or requirements set forth by the IRB coordination across PASSHE, such as reporting procedures or ongoing monitoring of participant data.
10
Throughout your research project, maintain open communication with the IRB coordination office and provide any updates or changes to your study as required.

Who needs IRB coordination across PASSHE?

01
Researchers and scholars conducting studies that involve human participants within the Pennsylvania State System of Higher Education (PASSHE) require IRB coordination.
02
Students and faculty members engaged in research projects as part of their academic coursework or professional endeavors may also need IRB coordination across PASSHE.
03
Any individual or organization affiliated with PASSHE and intending to conduct research involving human participants is responsible for obtaining IRB coordination as per the ethical guidelines and policies in place.
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IRB coordination across PASSHE refers to the process of aligning Institutional Review Board approvals for research projects involving multiple PASSHE institutions.
Principal Investigators leading research projects involving multiple PASSHE institutions are required to file IRB coordination across PASSHE.
To fill out IRB coordination across PASSHE, Principal Investigators must complete the necessary forms and submit them to the IRB office at each participating PASSHE institution.
The purpose of IRB coordination across PASSHE is to ensure ethical standards and compliance with regulations for research projects involving multiple PASSHE institutions.
The information reported on IRB coordination across PASSHE typically includes details of the research project, approval status from each institution's IRB, and any potential risks to participants.
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