Help the Institute for Clinical and Translational Science at the University of Iowa continue making new strides in medical research by citing the NIH CTSA program grant UM1TR004403. Epic users can access SlicerDicer via the Epic Reports Menu or via the search field in the upper right corner of the interface to: Get real-time patient counts. If you have a question regarding this policy or need help with training or implementation, please contact ICTS support or Kristy Mahan. The course is #WICTS2 Trainingīoth trainings are now available in HR Self Service Contact 0:00 51:20 CCTS BMI Learn at Lunch EPIC Slicer Dicer UKClinicalResearch 113 subscribers Subscribe 172 views 4 weeks ago BMI Learn at Lunch EPIC Slicer Dicer Title: Want to Learn Some. The course is #WICTS1.Īll clinical researchers who need to associate subjects in the EPIC medical record are required to take the policy awareness course titled "Associating a Research Subject in EPIC" once. Policy Awareness CourseĪll clinical researchers who participate in human subjects research are required to take the policy awareness course titled "Documentation of Participation in Study Protocol" once. The methodology and updates reports listed below describe the methods used to develop the risk-standardized readmission measures, and the 2023 measure updates and quality assurance activities. PolicyĪ copy of the policy IM-MR-06.21 DOCUMENTATION OF PATIENT PARTICIPATION AS A SUBJECT IN A RESEARCH PROTOCOL OR USE OF AN INVESTIGATIONAL MEDICATION, STUDY MEDICATION, INVESTIGATIONAL DEVICE, OR BIOLOGIC is located here. At the start of a search, an employee could enter a keyword to receive additional search criteria to consider. The following Slicer Dicer training modules are available: EPIC Self-service tutorial. This site contains resources to help researchers understand this new policy and follow good practices for implementing it. Epic Modules For Clinicians & Allied Health EpicCare Ambulatory. This research module also improves the management of the subjects who are in a study and simplifies billing of research funding sources. This policy leverages the availability of the “research module” in the Epic electronic health record to identify patients who are also subjects in research studies and provide information on the studies they are involved in. In an effort to improve the efficiency of clinical research studies and increase the safety of patients who participate in these studies, the policy on documenting patient participation as subject in research (UIHC policy policy IM-MR-06.21) has been updated. Data is the building block in all research, as results are only as good as the data upon which the conclusions were formed.
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