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Pepper dine University Protection of Human Participants in Research:Policies and Procedures ManualRevised November 17, 2009Pepperdine University Institutional Review Barnstable of Contents I. Introduction×7 A.

How to fill out protection of human participants

How to fill out protection of human participants

1. Step 1: Familiarize yourself with the guidelines and regulations set forth by the ethical review board or institutional review board (IRB) governing the protection of human participants.
2. Step 2: Obtain informed consent from the participants prior to their involvement in the study. This includes providing them with all necessary information about the study, potential risks and benefits, confidentiality, and their rights as research participants.
3. Step 3: Ensure that the participants' identities are protected and kept confidential throughout the study. Use codes or identifiers instead of personal identifying information whenever possible.
4. Step 4: Minimize any potential harm or discomfort to the participants by carefully designing the study and providing appropriate safeguards.
5. Step 5: Continuously monitor the participants' well-being during the study and be prepared to adjust or halt the research if any unforeseen negative consequences arise.
6. Step 6: Respect the participants' autonomy and right to withdraw from the study at any time without facing any negative consequences.
7. Step 7: Maintain accurate and detailed records of the study, including the participants' consent forms, data collected, and any changes made to the study protocol.
8. Step 8: Comply with all relevant ethical guidelines and regulations, and seek guidance from the IRB or other ethical review boards whenever needed.
9. Step 9: Regularly review and update your understanding and practices regarding the protection of human participants to ensure compliance with evolving standards.
10. Step 10: Publish and disseminate the findings of your study, giving credit to the contributions of the participants while maintaining their anonymity and confidentiality.

Who needs protection of human participants?

1. Researchers conducting studies involving human participants need protection of human participants.
2. Academic institutions and organizations conducting research involving human participants need protection of human participants.
3. Medical professionals conducting clinical trials or medical research involving human participants need protection of human participants.
4. Pharmaceutical companies and drug developers conducting trials or research involving human participants need protection of human participants.
5. Government agencies conducting studies or research involving human participants need protection of human participants.
6. Psychologists and social scientists conducting research involving human participants need protection of human participants.

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What is protection of human participants?

Protection of human participants refers to ensuring the safety, rights, and well-being of individuals who participate in research studies.

Who is required to file protection of human participants?

Researchers or institutions conducting research studies involving human participants are required to file protection of human participants.

How to fill out protection of human participants?

Protection of human participants forms typically require information on the study protocol, risks and benefits for participants, informed consent procedures, and steps taken to protect participants.

What is the purpose of protection of human participants?

The purpose of protection of human participants is to uphold ethical standards in research by safeguarding the rights, safety, and privacy of individuals involved in studies.

What information must be reported on protection of human participants?

Information such as study protocols, informed consent procedures, risk mitigation strategies, and data handling processes must be reported on protection of human participants.