Check C-CDA structure and content.
Assess CCD XML against C-CDA R2.1 and NCQA-oriented requirements.
Check CCDs against C-CDA R2.1 and NCQA-oriented rules. Locate issues, transform structural errors and retrieve corrected documents for quality workflows.
Browser-based evaluation. C-CDA validation. Document correction. Quality preparation.
Structural errors and inconsistent content can interrupt document exchange. Review the issues and corrections before passing a CCD to the next system.
Surface structural and content issues in incoming clinical documents.
Use explanations and document references to guide investigation.
Follow the transformation from a failed check to an output your team can inspect.
Evaluate document preparation alongside your reporting and submission requirements.
Keep document checks and transformation in the same workflow.
Assess CCD XML against C-CDA R2.1 and NCQA-oriented requirements.
Review explanations and document locations for failed checks.
Use the transformation workflow to generate a corrected CCD for review.
Download the transformed CCD for partner exchange or downstream processing.
Use corrected documents in preparation for HEDIS, DAV and digital quality workflows.
Filter validation and transformation metrics by date, user and operation.
Inspect the findings, run the available transformation and review the corrected document.
Build document checks into an existing quality-data pipeline.
Trial access includes API documentation. Review it for request formats and integration details.
Get Instant AccessExplore C-CDA validation workflows. For the foundations, explore FHIR resources, APIs and validation.
section/templateIdRequired template identifier is missing
patientRole/telecomReview the supplied contact value
ClinicalDocument/idDocument identifier is present
substanceAdministration/codeReview the entry against the selected rule
Illustrative sample data and results. This preview does not process uploaded data.
Try Care Compliance ValidatorUse synthetic or de-identified data only.
Explore the tool with representative test files before planning your production workflow.
Keep real patient data out of the trial environment.
Data transfers use encrypted connections.
The product does not retain uploaded source files.
Discuss your deployment and data-handling requirements with the Hgear team.
Support review across quality, clinical and data operations teams.
NCQA is a registered trademark of the National Committee for Quality Assurance. This product is not affiliated with or endorsed by NCQA.
This tool focuses on C-CDA XML documents, including CCDs. Its workflow validates documents and can transform structural issues before downstream use.
It helps prepare CCDs for NCQA-oriented, HEDIS, DAV and digital quality workflows. A tool result does not itself certify compliance or guarantee acceptance by a program.
APIs support document validation, transformation, corrected-document retrieval and activity metrics.
No. Use synthetic or de-identified CCDs in the trial environment.
Explore validation and correction using a representative test document.
Try Care Compliance ValidatorExplore how document preparation connects with validation and data quality across Hgear.
Explore platform validation