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http://motion.pratt.duke.edu/decisionsupport/index.html
Intelligent clinical decision support with Markov decision processes Dan Coroian, Kris Hauser ... Decision support tools have the promise to give clinicians better understanding of treatment outcomes and costs by integrating billions of electronic health record (EHR) datapoints with expert recommendations and best practices. This project aims ...
https://repository.duke.edu/
The Duke Digital Repository (DDR) is a service of Duke University Libraries that supports the activities of the University's faculty, researchers, students, and library staff by preserving, securing, and providing access to digital resources.
https://library.duke.edu/data/data-management/repository-support
About our program. The Duke University Libraries provides a formal research data repository and curation program in order to help researchers meet the FAIR Guiding Principles (Findable, Accessible, Interoperable and Reusable). Federal funders such as the National Institutes of Health (NIH) and scientific journals such as the Data Science Journal are committed to FAIR for both scientific ...
https://healthpolicy.duke.edu/events/developing-real-world-data-and-evidence-support-regulatory-decision-making
This conference on Developing Real-World Data and Evidence to Support Regulatory Decision-Making is funded by FDA through a cooperative agreement with the Duke-Margolis Center for Health Policy and will bring together leading experts to examine these questions, other topics addressed in the framework, as well as emerging topics in the ...
https://repository.duke.edu/catalog/0c42dc8a-0db2-4c82-a80b-b8b93c1c9957
411 Chapel Drive Durham, NC 27708 (919) 660-5870 Perkins Library Service Desk
https://irb.duhs.duke.edu/policies-and-regulations/policies/research-databases-specimen-repositories-and-contact-lists
The policy describes IRB requirements when investigators use databases and specimen repositories for research purposes. Databases/specimen repositories require consent and HIPAA authorization by subjects for the storage and potential future research use of their data/specimens, or a waiver of consent and HIPAA authorization by the IRB.
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