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This document provides guidelines for obtaining approval from the Auckland District Health Board (ADHB) Research Review Committee (RRC) for conducting research involving the organization. It includes
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How to fill out research approval guidelines

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How to fill out RESEARCH APPROVAL GUIDELINES

01
Begin with a clear project title at the top of the guidelines form.
02
Provide a concise abstract or summary of your research project.
03
State the purpose and objectives of your research clearly.
04
Outline the methodology, including research design, participant selection, and data collection methods.
05
Identify any potential ethical issues and how they will be addressed.
06
Specify the anticipated timeline for completing the research.
07
Include information on funding sources, if applicable.
08
Gather all necessary signatures and approvals from relevant parties.
09
Submit the completed guidelines form to the appropriate review board.

Who needs RESEARCH APPROVAL GUIDELINES?

01
Researchers conducting studies involving human subjects or sensitive data.
02
Institutions and organizations that require ethical review for research projects.
03
Students pursuing research as part of their academic programs.
04
Any individual seeking to ensure compliance with ethical research standards.
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Health Research Authority (HRA) brings together the HRA's assessment of governance and legal compliance with the independent ethical opinion by a Research Ethics Committee (REC) so you are required to submit only one application.
Where ethics approval has been obtained, the name of the approving body and the approval number/ID should be included in the manuscript. It is preferable for authors to include more detail than, for example, “Approval was obtained from the local ethics committee.”
Ethics Approval 1. Ethical approval for this study/case/case series was obtained from *NAME OF ETHICS COMMITTEE OR INSTITUTIONAL REVIEW BOARD (APPROVAL NUMBER/ID)*. 2. Ethical approval for this study was waived by *NAME OF ETHICS COMMITTEE OR INSTITUTIONAL REVIEW BOARD* because *REASON FOR WAIVER*.
Guiding Principles for Ethical Research Social and clinical value. Scientific validity. Fair subject selection. Favorable risk-benefit ratio. Independent review. Informed consent. Respect for potential and enrolled subjects.
Principles of research ethics PRINCIPLE ONE: Minimising the risk of harm. PRINCIPLE TWO: Obtaining informed consent. PRINCIPLE THREE: Protecting anonymity and confidentiality. PRINCIPLE FOUR: Avoiding deceptive practices. PRINCIPLE FIVE: Providing the right to withdraw.
Following points should be mentioned while writing the ethical consideration of a research proposal: Voluntary participation. Informed consent. Anonymity. Confidentiality. Potential for harm. Communication of results. Provision of medical assistance.
Where ethics approval has been obtained, the name of the approving body and the approval number/ID should be included in the manuscript. It is preferable for authors to include more detail than, for example, “Approval was obtained from the local ethics committee.”
1 Identify the ethical principles and standards. 2 Describe your research design and methods. 3 Discuss the ethical implications and challenges. 4 Provide references and appendices.

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RESEARCH APPROVAL GUIDELINES are a set of standards and procedures that researchers must follow to obtain permission for conducting research involving human participants, animals, or sensitive data.
All researchers, including faculty, graduate students, and any individuals conducting research that requires ethical consideration or oversight, must file the RESEARCH APPROVAL GUIDELINES.
To fill out the RESEARCH APPROVAL GUIDELINES, researchers should provide detailed information about their research project, including objectives, methodologies, participant recruitment, risks, and ethical considerations, and submit the completed forms to the appropriate review board.
The purpose of RESEARCH APPROVAL GUIDELINES is to ensure that research is conducted ethically, protecting the rights and welfare of participants and promoting scientific integrity.
Researchers must report information such as research objectives, methodology, potential risks and benefits, informed consent procedures, data management plans, and any funding sources.
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