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Summarize the attachments here. 12. Will participants receive inducements or rewards Give details. 13. 8. If research is conducted through an agency or institution complete the CityU Organizational Consent form to include the names contact information and contact persons for any institutions or agencies. Confidentiality I understand that participation is confidential to the limits of applicable privacy laws. Institutional Review Board Ethical Review Protocol City University of Seattle Ethics...

How to fill out ethical review protocol

How to fill out ethical review protocol

1. Read the guidelines provided by the ethical review board.
2. Ensure you have a clear understanding of the research study and its potential ethical implications.
3. Gather all the necessary information and materials required to complete the ethical review protocol.
4. Start by providing a concise and accurate summary of the research study.
5. Outline the objectives and aims of the study.
6. Describe the methodology and procedures that will be used in the research.
7. Identify any potential risks or harms that participants may experience during the study.
8. Explain the steps you will take to minimize and mitigate these risks.
9. Discuss the informed consent process and how you will ensure participants' understanding and voluntary participation.
10. Provide details on how participant confidentiality and privacy will be protected.
11. Outline any potential conflicts of interest that may arise during the study.
12. Include any additional information or documentation required by the ethical review board.
13. Review and edit the protocol to ensure clarity, accuracy, and adherence to ethical standards.
14. Submit the completed ethical review protocol to the appropriate ethical review board.
15. Await feedback and address any concerns or suggestions provided by the board.
16. Make any necessary revisions or additions to the protocol based on the feedback received.
17. Resubmit the revised protocol for final approval.
18. Upon receiving approval, continue with the research study while adhering to the ethical guidelines outlined in the protocol.

Who needs ethical review protocol?

1. Researchers conducting scientific studies involving human participants.
2. Academic institutions and universities requiring ethical review for research projects.
3. Medical professionals involved in clinical trials or experimental treatments.
4. Government agencies overseeing research or medical studies.
5. Non-profit organizations or foundations funding research studies.
6. Companies or industries conducting research that may impact human health or well-being.
7. Any individual or organization committed to ensuring ethical practices in research involving human subjects.

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What is ethical review protocol?

Ethical review protocol is a set of guidelines and procedures designed to ensure that research involving human subjects is conducted ethically and in compliance with regulatory requirements.

Who is required to file ethical review protocol?

Researchers and institutions conducting research involving human subjects are required to file an ethical review protocol.

How to fill out ethical review protocol?

To fill out an ethical review protocol, researchers must provide detailed information about their research design, methods, risks, benefits, and how they plan to protect the rights and welfare of human subjects.

What is the purpose of ethical review protocol?

The purpose of an ethical review protocol is to protect the rights and welfare of human subjects participating in research and to ensure that research is conducted in an ethical manner.

What information must be reported on ethical review protocol?

Information such as the research design, methods, potential risks and benefits to participants, informed consent process, and how participant confidentiality will be protected must be reported on an ethical review protocol.

What is the penalty for late filing of ethical review protocol?

The penalty for late filing of an ethical review protocol may vary depending on the specific institution or regulatory body overseeing the research, but it could result in delays in approval or even the suspension of the research project.