GIQuIC 2025 Qualified Clinical Data Registry (QCDR)
Since 2014, GIQuIC has been approved by CMS to serve as a Qualified Clinical Data Registry (QCDR). The QCDR reporting mechanism is a dynamic option that allows providers to report on GI-specific measures that are meaningful to their specialty practice and foster improvement in the quality of care provided to patients.
The GIQuIC QCDR is approved to report for individual eligible providers, groups, and virtual groups to the following performance categories:
GIQuIC 2025 QCDR Measures
To download the above document, please click here.
For more information about CMS’ Merit-based Incentive Payment System performance categories and the benefits of using the GIQuIC QCDR for reporting, click here.
GIQuIC 2025 Qualified Clinical Data Registry (QCDR)
2025 Reporting Year Deadlines/Checklist
To report to MIPS via the GIQuIC QCDR for the 2025 reporting year:
- Watch the following webinar that was conducted by the GIQuIC team and check back as we will post additional webinars throughout the reporting year:
- April 2, 2025 Webinar: Understanding MIPS Payment Adjustments: Navigating Your Reporting Options with GIQuIC
- Check physician MIPS eligibility: https://qpp.cms.gov/participation-lookup
If you have any questions about reporting to MIPS via the GIQuIC 2025 QCDR, please open a service ticket by clicking on Service Desk in the upper right-hand corner of the registry.
Clinicians and groups intending to report to CMS’ MIPS program via the GIQuIC QCDR must sign a Data Release Consent Form (DRCF) and submit a Form 1500. Please note that the DRCF process opens on May 5, 2025 and the deadline is July 6, 2025. There will be no exceptions to this deadline.
2025 GIQuIC MIPS Audit
To maintain its status as a Qualified Clinical Data Registry (QCDR) with CMS, GIQuIC must execute a Data Validation Plan to demonstrate to CMS that data submitted to the registry is true, accurate, and complete. Below are details about the process GIQuIC follows to conduct audits across the Quality, Promoting Interoperability, and Improvement Activities performance categories.
GIQuIC MIPS Quality Audit
If you are selected for a 2025 GIQuIC Quality Data Validation Audit and you have questions about the process, please open a service ticket in ZenDesk by clicking on your username in the top right-hand corner of the registry and then ARMUS Support. This will take you to ZenDesk where you can click on Submit a Request in order to open a service ticket.
GIQuIC MIPS Improvement Activities and Promoting Interoperability Audit
The audit relative to the Improvement Activities (IA) and Promoting Interoperability (PI) performance categories takes place in January of the year following the performance year.
Providers who submit data and attestations for the IA and PI performance categories via the GIQuIC 2025 QCDR must have relevant documentation (as per CMS guidelines) to substantiate this reporting. For those providers who have been randomly selected to participate in the audit, their GIQuIC Data Managers must provide the documentation to GIQuIC by the given deadline. If the provider has documentation that is not on the list of CMS suggested documents to substantiate this reporting, the provider(s) must provide it along with a valid reason for the alternate documentation.
IA and PI Audit Process:
- The GIQuIC support team will email the audit templates for each performance category to the Data Manager with a request to participate on a conference call with the GIQuIC team.
- During this initial call, the GIQuIC support team will review the audit template(s) with the Data Manager.
- The Data Manager will complete the audit template(s) and return the template(s) and supplemental materials to the GIQuIC support team (via secure email).
- Following a review of the audit materials, the GIQuIC support team will schedule a second call, if necessary, to address any questions or deficiencies.
- GIQuIC will notify the Data Manager when the IA and PI portion of the audit has been successfully completed.