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Honest broker protocol streamlines research access to data while safeguarding patient privacy
Scott A Silvey1, Scott Andrew Silvey, Janet Schulte
1Information Warehouse, Ohio State University Medical Center, Columbus, Ohio, USA.
AMIA ... Annual Symposium Proceedings. AMIA Symposium
|November 13, 2008
Summary
The Honest Broker Protocol simplifies accessing de-identified clinical data for non-FDA research. This streamlines the process, saving investigators significant time and effort compared to traditional IRB approval methods.
Area of Science:
- Health Services Research
- Clinical Data Management
Background:
- Accessing de-identified clinical data is crucial for non-FDA research.
- Traditional Institutional Review Board (IRB) approval processes can be time-consuming and resource-intensive for researchers.
Purpose of the Study:
- To introduce and evaluate the Honest Broker Protocol as a streamlined mechanism for data access.
- To reduce the burden on investigators seeking de-identified clinical data for research.
Main Methods:
- Implementation of the Honest Broker Protocol at Ohio State University Medical Center.
- Utilizing de-identified clinical data for non-FDA regulated research.
Main Results:
- The protocol offers a simplified pathway for investigators.
- Reduces the need for extensive protocol development for IRB review.
Conclusions:
- The Honest Broker Protocol effectively facilitates access to de-identified clinical data.
- This mechanism saves valuable investigator time and resources for non-FDA research.
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