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Host North Shore LIE School of Medicine Application for IRB Review of Educational Research Name: Phone #: Email Address: Title of Research: Purpose of Research (150 words or fewer): Type of Review
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How to fill out application for irb review

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01
Start by gathering all the necessary information: Before filling out the application for IRB (Institutional Review Board) review, make sure you have all the relevant details ready. This includes information about the research project, the researchers involved, the study population, and any potential risks or benefits.
02
Familiarize yourself with the IRB guidelines: Each institution may have its own specific guidelines for the IRB application process. It is important to thoroughly read and understand these guidelines to ensure that your application meets all the necessary requirements. Pay close attention to the sections that outline what information needs to be included and the format in which it should be presented.
03
Provide a clear project description: In the application, clearly describe the research project and its objectives. Explain the research question or hypothesis, the methods that will be used, and the anticipated outcomes. Be sure to use language that is easily understandable to both the review board members and the general public.
04
Detail the study population and recruitment process: Describe the population that will be involved in the study, including any specific demographics or characteristics. Explain how the participants will be recruited, ensuring that the methods used are ethical and in line with the IRB guidelines.
05
Address potential risks and benefits: In the application, identify and discuss any potential risks or benefits associated with the research. This could include physical, psychological, or social risks that participants may face during the study. Similarly, highlight any potential benefits that may arise from the research, such as advancing scientific knowledge or improving patient care.
06
Outline the informed consent process: Clearly explain the process of obtaining informed consent from study participants. Describe how you will ensure that participants fully understand the nature of the study, its purpose, risks, benefits, and their rights as participants. Include copies of any consent forms or information sheets that participants will receive.
07
Include a data management plan: Provide details on how you will collect, store, and handle the data obtained from the study. Explain how you will ensure the confidentiality and privacy of the participants, as well as how long you intend to retain the data.
08
Specify the personnel involved: Clearly list all the researchers involved in the project, including their qualifications and roles. This includes the principal investigator, co-investigators, research assistants, and any external collaborators.
09
Discuss the timeline and budget: Outline the anticipated timeline for the study, including the duration of participant recruitment, data collection, and data analysis. Additionally, provide a budget that highlights any necessary resources, personnel costs, or funding sources required for the research.
10
Who needs an IRB review: The application for IRB review is typically required for any research involving human subjects. This includes both biomedical and social/behavioral studies that aim to collect data from or about individuals. Various institutions, such as universities or healthcare organizations, have their own processes to determine whether a study requires IRB review.
Remember, it is important to consult your institution's specific guidelines and resources when filling out the application for IRB review, as they may have additional requirements or recommendations.
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The application for irb review is a formal submission required to seek approval from an Institutional Review Board (IRB) for research involving human subjects.
Researchers conducting studies involving human subjects are required to file an application for irb review.
The application for irb review typically involves providing detailed information about the research study, including its purpose, methodology, risks and benefits, and how participants will be recruited and protected.
The purpose of the application for irb review is to ensure that research involving human subjects is conducted ethically and in compliance with regulations to protect the rights and welfare of participants.
Information such as study protocols, participant consent forms, potential risks and benefits, data handling procedures, and researcher qualifications must be reported on the application for irb review.
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