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FOR IRB USE ONLY
APPROVED BY: IRB01
IRB ID #: 201301763
APPROVAL DATE: 09/04/18
EXPIRATION DATE: 08/23/19INFORMED CONSENT DOCUMENT
Project Title:
A Randomized, DoubleClick, Placebo Controlled Trial
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How to fill out irb-01 homeinstitutional review boarduniversity
How to fill out irb-01 homeinstitutional review boarduniversity
01
Obtain the IRB-01 form from your institution's website or IRB office.
02
Fill out the required fields such as researcher name, project title, and contact information.
03
Provide a detailed description of the research project including the purpose, methods, and potential risks or benefits.
04
Include information on how subjects will be recruited, consent obtained, and data protected.
05
Submit the completed IRB-01 form along with any supporting documents to the institutional review board for approval.
Who needs irb-01 homeinstitutional review boarduniversity?
01
Researchers planning to conduct research involving human subjects at a university or institution need to fill out IRB-01 home/institutional review board form.
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What is irb-01 homeinstitutional review boarduniversity?
The IRB-01 homeInstitutional Review BoardUniversity is a committee responsible for ensuring the protection of human subjects in research conducted at the institution.
Who is required to file irb-01 homeinstitutional review boarduniversity?
Researchers conducting studies involving human subjects are required to file IRB-01 forms with the Institutional Review Board.
How to fill out irb-01 homeinstitutional review boarduniversity?
Researchers need to provide detailed information about their study, including the purpose, methods, risks, and benefits, in the IRB-01 form.
What is the purpose of irb-01 homeinstitutional review boarduniversity?
The purpose of IRB-01 is to ensure that research involving human subjects is ethically conducted and that the rights and welfare of participants are protected.
What information must be reported on irb-01 homeinstitutional review boarduniversity?
Researchers must report detailed information about the study design, recruitment procedures, informed consent process, data collection methods, and risk mitigation strategies.
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