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One Platform for AML ComplianceContents01 | CONTENTS03FROM SMALL BEGINNINGS05SMART SYSTEMS YOU CAN RELY on ON07DATA DRIVEN OUTCOMES09FUNCTIONALITY OVERVIEW11THE SERVICE DIMENSION13DEALING WITH DOCUMENTS15NO
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01
Review the guidelines provided by the panel in order to determine which data points are relevant for assessing clinical impact
02
Fill out the impact assessment form by providing specific examples of how the panel-based information has influenced decision making in patient care
03
Include any supporting evidence such as patient outcomes or changes in treatment plans
04
Specify any limitations or challenges encountered when assessing the clinical impact of panel-based information

Who needs clinical impact of panel-based?

01
Healthcare professionals who are involved in using panel-based information to make clinical decisions for patients
02
Researchers who are evaluating the effectiveness of panel-based testing in guiding patient care
03
Policy makers who are interested in understanding the implications of incorporating panel-based information into healthcare practices
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The clinical impact of panel-based refers to the effects and implications of using a panel of genetic tests to diagnose or treat a patient.
Healthcare professionals or researchers who have conducted panel-based testing are required to file the clinical impact report.
The clinical impact report for panel-based testing can be filled out by documenting the results, interpretations, and implications of the genetic tests.
The purpose of the clinical impact report is to provide insight into how the results of panel-based testing can inform patient care decisions.
The clinical impact report should include details on the genetic tests performed, the results obtained, and the impact on patient management.
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