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AUM IRB Protocol 6.2013AUM Research Protocol Review Form Institutional Review Board for Research Involving Human Subjects Office of Sponsored Programs (OSP), 109 Administration Bldg 334.2443250 For
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How to fill out aum irb protocol 6
How to fill out aum irb protocol 6
01
Gather all necessary information and materials required to complete the AUM IRB Protocol 6 form.
02
Fill out the cover sheet with basic information such as the title of the research project, name of the principal investigator, and contact information.
03
Provide a detailed description of the research project including the research question, methodology, and participant information.
04
Include any risks and benefits associated with the research project as well as a plan for participant recruitment and informed consent procedures.
05
Complete all required sections of the form accurately and thoroughly, making sure to adhere to AUM IRB guidelines and regulations.
06
Review the completed form for accuracy and completeness before submitting it to the AUM IRB for review and approval.
Who needs aum irb protocol 6?
01
Researchers conducting research projects involving human participants at Auburn University at Montgomery (AUM) need to fill out and submit AUM IRB Protocol 6.
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What is aum irb protocol 6?
AUM IRB Protocol 6 is a specific set of guidelines and protocols established for Institutional Review Boards (IRBs) to evaluate and manage research activities involving human subjects.
Who is required to file aum irb protocol 6?
Researchers and institutions conducting studies that involve human subjects and fall under the jurisdiction of an IRB are required to file AUM IRB Protocol 6.
How to fill out aum irb protocol 6?
Filling out AUM IRB Protocol 6 involves completing the provided documentation with details of the research study, including objectives, methodologies, subject recruitment strategies, and informed consent processes, followed by submitting it to the IRB for review.
What is the purpose of aum irb protocol 6?
The purpose of AUM IRB Protocol 6 is to ensure ethical standards in research involving human subjects, safeguarding participants’ rights and welfare while promoting responsible research conduct.
What information must be reported on aum irb protocol 6?
The information required on AUM IRB Protocol 6 includes study title, principal investigator details, research objectives, study design, participant selection criteria, potential risks, benefits, informed consent processes, and data management.
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