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Suspected Unanticipated Problem Report Form Send this form to: Lori Robinson, IRB Coordinator Guthrie Foundation Robinson×Gloria×Guthrie.org Does the incident, experience, or outcome meet all the
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01
Obtain the necessary forms for filling out the Lori Robinson IRB Coordinator. These forms can usually be found on the institution's website or obtained from the IRB office.
02
Start by filling out the personal information section, including your name, contact details, and institutional affiliation.
03
Provide a brief overview of your research project and its objectives.
04
Clearly state the research question or hypothesis that you will be addressing in your study.
05
Describe the study design, methodology, and data collection techniques that you will be using.
06
Discuss the potential risks and benefits of your research and how you plan to mitigate any risks.
07
Include a section on the informed consent process, detailing how you will obtain consent from participants and ensure their understanding of the study.
08
If applicable, provide information on any recruitment methods you plan to use to gather participants for your study.
09
Describe the data analysis techniques you will employ and how you plan to protect the privacy and confidentiality of participants.
10
Finally, review your completed Lori Robinson IRB Coordinator form to ensure all sections are filled out accurately and submit it to the IRB office for review and approval.

Who needs lori robinson irb coordinator?

01
Researchers who are conducting studies involving human subjects and are affiliated with an institution that requires IRB approval would need a Lori Robinson IRB Coordinator. This coordinator helps ensure that the study follows ethical guidelines and regulations set by the IRB and protects the rights and welfare of the participants.

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