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Currently, samples are only available to
Ohio University researchers and their associates. In the
future, these samples will be available to all approved
researchers. Please check back to this website for
updated information as that becomes available.
Any investigators requesting access to
specimens from the Biorepository is required to:
- Submit a formal proposal to the OU Biorepository Advisory Board.
- Submit a formal proposal to the Ohio University Institutional Review Board (IRB) for approval.
- Submit a formal proposal to the University Medical associates (UMA) Research Committee for final approval.
Upon obtaining all approvals, the
investigators will be required to sign a Limited Data
Set Agreement and complete the OU HIPAA training
program. The Limited Data Set Agreement will stipulate
what summary clinical information will be provided from
the Ohio University Diabetes/Endocrine Diseases Database
and will set a time limit on their access to this data
set and specimens from the Biorepository. Only the
Biorepository Coordinator or a designee will have direct
access to the database and be allowed to mine this
database to create a list of potential research samples.
The requested specimens are retrieved from the
Biorepository freezers and provided to the investigators
at that time with necessary encrypted, summary clinical
information. We ask that
investigators acknowledge the contributions made by the
Ohio University Diabetes/Endocrine Diseases
Biorepository in all publications and presentations
resulting from the use of these samples. Recommended
wording be as follows: "samples for this project were
provided by the Ohio University Diabetes/Endocrine
Diseases Biorepository." |