Participation by a physician or other clinician in systematic clinical database registry that includes consensus endorsed quality measures

The clinician participates in a systematic qualified clinical database registry capable of the following:
a. Physician or other clinician submits standardized data elements to registry
b. Data elements are applicable to consensus endorsed quality measures
c. Registry measures shall include at least two (2) representative NQF consensus endorsed measures for registry's clinical topic(s) and report on all patients eligible for the selected measures.
d. Registry provides calculated measures results, benchmarking, and quality improvement information to individual physicians and clinicians.
e. Registry must receive data from more than 5 separate practices and may not be located (warehoused) at an individual group’s practice. Participation in a national or state-wide registry is encouraged for this measure.
f. Registry may provide feedback directly to the provider’s local registry if one exists.