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Policies and Procedures Manual
for Human Subjects
Institutional Review BoardAdopted: MARCH 2001
Amended: August 2013, April 2015, February 2017Guidelines16/12/2017University of Findlay
IRB Policies
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How to fill out for human subjects
How to fill out for human subjects
01
Start by reviewing the purpose and objectives of the study.
02
Obtain the necessary approval from an Institutional Review Board (IRB) or ethics committee.
03
Prepare the informed consent form, ensuring it includes all required information.
04
Recruit potential human subjects based on the study's eligibility criteria.
05
Schedule and conduct face-to-face or online interviews with the subjects.
06
Collect and record data according to the study's protocols.
07
Ensure the privacy and confidentiality of the subjects' personal information.
08
Analyze the collected data using appropriate statistical methods.
09
Interpret the results and draw conclusions based on the findings.
10
Prepare a comprehensive report detailing the study's methodology, results, and conclusions.
Who needs for human subjects?
01
Researchers conducting scientific studies
02
Medical professionals conducting clinical trials
03
Social scientists conducting surveys or experiments
04
Psychologists conducting research on human behavior
05
Educational institutions conducting studies on students
06
Market researchers conducting consumer studies
07
Government agencies conducting public health research
08
Pharmaceutical companies testing new drugs on human volunteers
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What is for human subjects?
For human subjects refers to any research involving individuals as participants.
Who is required to file for human subjects?
Researchers conducting studies with human subjects are required to file.
How to fill out for human subjects?
Researchers must carefully complete the necessary forms and provide all required information.
What is the purpose of for human subjects?
The purpose of filing for human subjects is to ensure the protection and ethical treatment of individuals participating in research studies.
What information must be reported on for human subjects?
Information such as the study protocol, potential risks and benefits, informed consent process, and confidentiality measures must be reported.
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