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Human Participants Research Revised Protocol Form1REVISED RESEARCH PROTOCOL FOR APPROVED AND CURRENTLY ACTIVE EXEMPT OR EXPEDITED PROTOCOLS FOR THE COLLEGE OF SAINT ROSE INSTITUTIONAL REVIEW BOARD

How to fill out exempt review research protocol

How to fill out exempt review research protocol

1. Start by gathering all the necessary information and documents required for the exempt review research protocol.
2. Clearly define the research objectives and hypotheses to be tested in the protocol.
3. Provide a detailed explanation of the research methodology to be used, including the study design, data collection procedures, and analysis methods.
4. Describe the target population or sample size for the research study.
5. Specify any potential risks or benefits to participants and outline the steps taken to minimize risk.
6. Clearly state the informed consent process and how participants' confidentiality will be protected.
7. Include a plan for data management and storage to ensure privacy and security.
8. Provide a timeline for the research project, including start and end dates for data collection and analysis.
9. Attach any necessary supporting documents, such as informed consent forms, questionnaires, or recruitment materials.
10. Review the protocol for accuracy, completeness, and adherence to ethical guidelines before submission.

Who needs exempt review research protocol?

1. Researchers or institutions conducting research studies that meet the criteria for exemption as defined by the relevant regulatory bodies and ethical guidelines.
2. Exemption from review is usually granted for research that involves minimal risk to participants, does not involve sensitive or identifiable information, and falls within specific categories specified by the regulatory bodies.
3. Individuals or organizations planning to publish or present the research findings may also need an exempt review research protocol to demonstrate compliance with ethical standards.

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What is exempt review research protocol?

An exempt review research protocol refers to a type of research study that is exempt from the usual requirements of institutional review board (IRB) review due to the nature of the research, which poses minimal risk to participants.

Who is required to file exempt review research protocol?

Researchers conducting studies that meet specific criteria for exempt status are required to file an exempt review research protocol with the applicable institutional review board (IRB).

How to fill out exempt review research protocol?

To fill out an exempt review research protocol, researchers must provide detailed information about the study design, methods, participant criteria, and any potential risks or benefits associated with the research, following specific guidelines provided by the IRB.

What is the purpose of exempt review research protocol?

The purpose of the exempt review research protocol is to ensure that studies qualifying for exempt status are reviewed for compliance with ethical standards while streamlining the process for low-risk research.

What information must be reported on exempt review research protocol?

Information reported on an exempt review research protocol typically includes the study title, principal investigator details, study objectives, methodology, data collection procedures, and consent process, among other relevant aspects.