Your office should reach out to your state registry to set up a connection (this occurs outside of EZDERM). Once you are enrolled with a registry, you can use EZDERM to document the details that are required in the cancer report. After this report is finished and reviewed, it can be generated and uploaded to the Registry.
The process differs from state-to-state, but the general workflow is defined with the following steps:
1. Clinician registers in the Cancer Registry for MU3/MIPS program. Registration is done on Registry end and it is important that registration is completed within 60 days after the start of the MIPS performance period.
2. After completed registration, clinician sends test messages (created through EZDERM) that should be validated by the Registry.
3. Once the Registry finishes validation, production is ready to be started.
State and Local Public Health Agencies (PHAs) Resource
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