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PEPPERMINT IRB CONTINUING REVIEW FORM This form must be completed if data collection or analysis will still be in progress one year past last IRB approval. The IRB is required by federal regulations
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How to fill out irb frequently asked questions

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How to fill out irb frequently asked questions

01
Start by visiting the IRB website
02
Look for the 'FAQ' section on the website
03
Click on the 'FAQ' link to access the frequently asked questions
04
Read through the questions and their corresponding answers
05
If you have a specific question, use the search bar to find relevant FAQs
06
If you cannot find an answer to your question, contact the IRB directly for assistance

Who needs irb frequently asked questions?

01
Researchers who are planning to conduct studies that involve human subjects
02
Students who are working on research projects that require IRB approval
03
Institutional review board members or administrators who need to familiarize themselves with common questions and answers
04
Anyone interested in understanding the IRB process and guidelines for human subjects research

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IRB frequently asked questions refer to common queries and clarifications related to Institutional Review Boards, their processes, and requirements for research involving human subjects.
Researchers and institutions conducting studies involving human participants are required to file IRB applications and may refer to frequently asked questions for guidance.
To fill out IRB frequently asked questions, researchers should review the guidelines provided by their institution's IRB and answer based on their specific study details.
The purpose is to provide guidance and clarify the IRB process for researchers, ensuring compliance and protection for human subjects in research.
Information that should be reported includes study design, participant recruitment, informed consent processes, and any potential risks to participants.
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