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IRB APPROVED AS MODIFIED Jan 03, 2021RESEARCH SUBJECT INFORMATION AND CONSENT FORM Normal Donor Blood Product Collections NFL DONOR_BLOOD_002 WIRE Protocol #20151321SPONSOR:Blood works NorthwestINVESTIGATOR:David
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01
Access the human research protection program website or contact program representative.
02
Obtain the required modification forms and guidelines.
03
Fill out the modification form with accurate and detailed information regarding the changes to the research protocol.
04
Provide any additional documentation or materials requested to support the modification request.
05
Submit the completed modification form and supporting documents to the program for review and approval.

Who needs modificationhuman research protection program?

01
Researchers conducting human subjects research
02
Institutional review boards overseeing research studies involving human participants
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The modifications to the human research protection program involves changes made to the safeguards in place for research involving human subjects.
Researchers and institutions conducting human subjects research are required to file modifications to the research protection program.
Modifications to the human research protection program can be filled out by providing detailed information about the changes being made and the reasons for those changes.
The purpose of the modifications to the human research protection program is to ensure that the rights and wellbeing of human subjects are protected during research experiments.
Information such as the changes to the research protocol, consent forms, recruitment procedures, and any potential risks to human subjects must be reported on modifications to the human research protection program.
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