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Revised 2/2/2018 CONSENT FORMS: Consent forms are required for most research involving human subjects. Please see the instructions for consent forms in the IRB Handbook, Section 6, found on the University
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How to fill out new irb application

01
Read the instructions on the new IRB application form carefully.
02
Gather all necessary information and documents, such as study protocols, consent forms, and supporting documents.
03
Start by filling out the top section of the application, providing the study title, principal investigator's name, and contact information.
04
Proceed to fill out the study information section, providing details about the study design, objectives, and methods.
05
Fill out the participant demographics section, including information about the target population, recruitment process, and inclusion/exclusion criteria.
06
Complete the section on study risks and benefits, clearly explaining the potential risks to participants and the potential benefits of the study.
07
Provide detailed information about the informed consent process and how participants will be recruited and consented.
08
Fill out the section on data collection and analysis, outlining the methods that will be used to collect and analyze data.
09
Include any additional documentation required, such as consent form templates, recruitment materials, or data collection instruments.
10
Review the completed application form for any errors or missing information, ensuring all necessary signatures and dates are included.
11
Submit the completed IRB application form, along with any supporting documents, to the appropriate IRB committee.
12
Follow up with the IRB committee for any additional questions or requests for revisions.

Who needs new irb application?

01
Researchers planning to conduct human subject research that falls under the jurisdiction of an Institutional Review Board (IRB) need to fill out a new IRB application.
02
Institutions and organizations that have an IRB may require their researchers to submit a new IRB application for review and approval before initiating any new research study involving human subjects.
03
Individuals or groups conducting research funded by government agencies or private foundations may need to complete a new IRB application as part of the funding requirements.
04
Graduate students, undergraduate students, and postdoctoral researchers who are conducting independent research projects with human subjects may also need to fill out a new IRB application.
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New IRB application is a form submitted to an Institutional Review Board (IRB) for approval before conducting research involving human subjects.
Researchers and institutions conducting research involving human subjects are required to file a new IRB application.
New IRB applications can be filled out online through the IRB portal, following the provided guidelines and instructions.
The purpose of the new IRB application is to ensure the protection of human subjects in research studies and compliance with ethical guidelines.
New IRB applications must include details on the research protocol, informed consent process, potential risks to subjects, and safeguards in place.
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