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ATTACHMENT 3 PROTOCOL # IRB Office Use Only MARYLAND DEPARTMENT OF HEALTH AND MENTAL HYGIENE OFFICE OF THE INSPECTOR GENERAL INSTITUTIONAL REVIEW BOARD FORM 1 (DHH 2124) PROTOCOL STATUS: NEW APPLICATION
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How to fill out an institutional review board form:

01
Start by carefully reading and understanding the instructions provided with the form. Make sure you are familiar with the purpose of the form and what information is required.
02
Begin filling out the form by providing your personal information such as your name, contact details, and institutional affiliation. This information is essential for identification purposes.
03
Next, provide details about the research project you are conducting. This includes the title of the study, a brief summary or abstract, and a clear description of the objectives and goals of the research.
04
Specify the methodology and procedures you will be using in your study. This includes information about the participants, any potential risks or benefits involved, and the data collection and analysis techniques you will employ.
05
If applicable, include information about any funding sources or conflicts of interest that could influence the research. Transparency is crucial in maintaining the integrity of the study.
06
Ensure that you address ethical considerations such as obtaining informed consent from participants, protecting their privacy and confidentiality, and addressing any potential harm or discomfort they may experience.
07
If you are involving human subjects in your research, provide details about the recruitment process, the informed consent procedures, and any measures you will take to minimize potential risks to participants.
08
Finally, gather any additional documents or supporting materials required by the institutional review board (IRB) and submit them along with the completed form. These may include consent forms, questionnaires, interview scripts, or any other relevant materials.

Who needs an institutional review board form?

01
Researchers conducting studies involving human subjects are generally required to complete an institutional review board form. This ensures that ethical standards are upheld and the rights and well-being of participants are protected.
02
Academic institutions, hospitals, and other research organizations usually have an IRB in place to review and approve research projects to ensure compliance with ethical guidelines. Researchers affiliated with these institutions will need to submit the IRB form for committee review.
03
Funding agencies may also require researchers to obtain IRB approval for their studies before they can receive funding. This is to ensure that research involving human subjects meets appropriate ethical standards.
In summary, filling out an institutional review board form involves providing detailed information about your research project and addressing ethical considerations. Researchers conducting studies involving human subjects typically need to complete this form, and it is usually required by academic institutions, research organizations, and funding agencies to ensure compliance with ethical guidelines.
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The institutional review board form is a document used to request approval for research involving human subjects.
Researchers conducting studies involving human subjects are required to file the institutional review board form.
The institutional review board form is typically completed by providing information about the study design, recruitment methods, risks to participants, and consent procedures.
The purpose of the institutional review board form is to ensure that research involving human subjects is conducted ethically and in compliance with regulations.
The institutional review board form typically requires information on study objectives, participant recruitment, data collection methods, risks and benefits, and consent procedures.
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