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This form is to be used for submitting modifications, continuation requests, or final reports for research projects involving human subjects. It requires the signature of the Principal Investigator
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How to fill out MICHIGAN TECH - INSTITUTIONAL REVIEW BOARD (IRB) APPLICATION FOR MODIFICATION / CONTINUATION OR FINAL REPORT FOR PROJECT COMPLETION

01
Begin by downloading the Michigan Tech IRB Application for Modification/Continuation or Final Report form from the official website.
02
Read the instructions carefully to understand the requirements for modifications, continuation, or final reporting.
03
Fill out the project title and principal investigator's information at the top of the form.
04
Indicate the type of application you are submitting: modification, continuation, or final report.
05
Provide a detailed description of the modifications or updates to your project, if applicable.
06
Include the reason for continuation or any relevant findings if submitting a final report.
07
Ensure all required signatures are obtained from the principal investigator and any co-investigators.
08
Submit the completed form via the appropriate channel as instructed on the form.

Who needs MICHIGAN TECH - INSTITUTIONAL REVIEW BOARD (IRB) APPLICATION FOR MODIFICATION / CONTINUATION OR FINAL REPORT FOR PROJECT COMPLETION?

01
Researchers and faculty members at Michigan Tech who are conducting research involving human subjects.
02
Any project that has received IRB approval and is undergoing changes or is approaching completion.
03
Individuals who need to continue their approved research or wish to report on its completion.
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People Also Ask about

The terminology used to describe a change to a protocol may vary, including terms such as modification, amendment or revision. All modifications to currently approved research studies are required to have IRB review and approval prior to implementation.
A principal investigator may not implement any changes to an approved study (including to the protocol or informed consent document) without prior IRB review and approval, unless the change is necessary to eliminate apparent immediate hazards to the subjects.
Modifications are study changes that should be submitted to the IRB for approval prior to implementing except when an immediate change is needed to eliminate or alleviate an apparent hazard or risk to subjects. Study changes without prior IRB approval must be submitted as Reportable New Information.
The Institutional Review Board (IRB) is an administrative body established to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated.
IRB must review all projects that meet the definition of research and that involve human subjects prior to any data collection to determine the appropriate level of review, and, as appropriate, approve them. There are three major types of review: Exempt, Expedited, and Full.
Continuing review provides the IRB with an opportunity to determine whether there is any new information that should be considered to represent such a significant new finding and therefore be communicated to subjects who have already enrolled in the research (e.g., important new toxicity information or new adverse

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The Michigan Tech Institutional Review Board (IRB) Application for Modification/Continuation or Final Report for Project Completion is a form used by researchers to report changes to ongoing research, request an extension, or submit a final report upon completing their research study.
All researchers conducting studies involving human subjects at Michigan Tech are required to file this application when making modifications to their research, seeking continuance, or finalizing project completion.
Researchers should follow the specific instructions provided on the form, ensuring to clearly outline the modifications, justification for continuance, or completion details, and provide all necessary documentation as required by the IRB guidelines.
The purpose of this application is to ensure the continued protection of human subjects, allow IRB to assess any changes to study protocols, monitor ongoing research, and properly document the completion of research activities.
Researchers must report details regarding the nature of modifications, reasons for continuation, any adverse events that occurred, updated consent processes, and final outcomes or findings of the research.
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