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TOUCH MEMORIAL INSTITUTE FOR MEDICAL RESEARCH (NMI MR) Office Use Only COLLEGE OF HEALTH SCIENCES, UNIVERSITY OF GHANA, LEON Protocol Number: INSTITUTIONAL REVIEW BOARD FORM F STUDY DEVIATION FORM
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How to fill out form F study deviation:

01
Start by carefully reading the instructions provided with the form. Understand the purpose and requirements of the study deviation.
02
Fill in your personal information accurately, including your name, contact details, and any identification numbers required.
03
Provide information about the study you are involved in, such as the title, study ID, and other relevant details. Double-check this information for accuracy.
04
Explain the reason for the study deviation clearly and concisely. Include any supporting documents or evidence if required.
05
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Keep a copy of the completed form for your records and submit the original to the appropriate authority.

Who needs form F study deviation?

01
Researchers or individuals conducting studies that deviate from the approved protocol may need to fill out form F study deviation. This form is typically required in research settings where deviations from the original study plan may occur.
02
Institutional review boards (IRBs) or ethics committees may require the submission of form F study deviation to assess and approve any requested changes to the study protocol.
03
Participants or subjects involved in the study may also need to be informed about and consent to any proposed deviations, which may be documented using form F study deviation.
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Form F Study Deviation is a document used to report any deviations from the approved study protocol during a clinical trial.
The Principal Investigator or the sponsor of the clinical trial is required to file Form F Study Deviation.
Form F Study Deviation should be filled out by providing details of the deviation, its impact on the study, actions taken, and plans for resolution.
The purpose of Form F Study Deviation is to ensure transparency and documentation of any deviations from the approved study protocol.
Information such as the date and nature of the deviation, its impact on the study participants, actions taken, and plans for resolution must be reported on Form F Study Deviation.
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