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Page 1 of 7UW HS IRB #20151376 UNIVERSITY OF WISCONSINMADISON Subject CONSENT to Participate in Research And AUTHORIZATION to Use and/or Disclose Identifiable Health Information for Research Title
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To fill out UW HS-IRB 2015-1376, follow these steps:
02
Download the form from the official website of the UW HS-IRB.
03
Read the instructions carefully to understand the purpose and requirements of the form.
04
Provide your personal information such as name, contact details, and any relevant affiliations.
05
Clearly state the title of your research project and provide a brief summary or abstract.
06
Indicate the primary investigator and any co-investigators involved in the study.
07
Describe the research methodology, including the study design, data collection methods, and analysis procedures.
08
Provide details about potential risks and benefits associated with the study for participants.
09
Explain how you plan to obtain informed consent from participants and maintain confidentiality of their personal information.
10
Include any relevant supporting documents such as participant consent forms, surveys, or interview scripts.
11
Review the completed form for accuracy and completeness before submitting it to the UW HS-IRB office.

Who needs uw hs-irb 2015-1376?

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Anyone who wishes to conduct research involving human subjects at the University of Washington (UW) may need to fill out UW HS-IRB 2015-1376. The form is specifically designed for researchers who need to obtain approval from the Human Subjects Institutional Review Board (HS-IRB) at UW. This includes faculty, staff, students, or external researchers who are affiliated with the university and plan to conduct research that involves human participants. It is important to review the specific guidelines and criteria set forth by the UW HS-IRB to determine if this form is applicable to your research project.
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uw hs-irb 1376 is a form used for submitting human subjects research protocols to the Institutional Review Board (IRB) at the University of Washington.
Researchers conducting human subjects research at the University of Washington are required to file uw hs-irb 1376.
To fill out uw hs-irb 1376, researchers must provide detailed information about the research protocol, potential risks and benefits to participants, and consent procedures.
The purpose of uw hs-irb 1376 is to ensure that all human subjects research conducted at the University of Washington meets ethical and regulatory standards to protect participants.
Information such as the research protocol, potential risks and benefits to participants, consent procedures, and any conflicts of interest must be reported on uw hs-irb 1376.
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