Validate and Transform CCD Documents for NCQA, HEDIS, and Digital Quality Measures
Use our Care Compliance Validator and Transformer to ensure C-CDA documents meet NCQA standards and are ready for use in HEDIS reporting, dQM pipelines, and Data Aggregator Validation (DAV) workflows.
No setup. No code. Just transformation.
Try the Free Care Compliance Validator
Start validating and transforming C-CDA documents in seconds. No installation or setup needed.
Why NCQA Compliance and HEDIS Readiness Remain a Challenge
As NCQA shifts to digital-first quality measurement, organizations must prepare data that is not only standards-aligned, but also submission-ready. CCDs generated across multiple systems often contain structural issues, non-standard codes, and missing sections.
Manual review and correction are time-consuming and error-prone. More importantly, CCDs that fail validation cannot be used as supplemental data in HEDIS reporting or DAV programs, unless they are corrected and traceable.
The Care Compliance Validator and Transformer eliminates this burden by validating incoming CCDs, correcting issues automatically, and producing compliant documents ready for audit, analytics, and quality programs.
The Solution Validate, Correct, and Align with NCQA Standards A One-Stop Tool for NCQA, HEDIS, and Digital Quality Preparation
Validate C-CDA Files Against NCQA Rules
Upload any CCD (.xml) and check it for structural and content compliance with HL7 C-CDA R2.1 and NCQA’s evolving standards.
Enable HEDIS and dQM Readiness
Corrected CCDs are structured to support downstream use in digital quality measures, FHIR mapping, and DAV-aligned data submission.
Pinpoint and Understand Validation Errors
If a file fails validation, receive a clear explanation and the exact location of each issue.
Download Corrected Files Instantly
Receive a validated CCD ready for supplemental data use, partner sharing, or submission.
Automatically Transform Non-Compliant Files
Use the Transform feature to correct structural errors and generate an NCQA-aligned CCD ready for reuse.
Track Performance and Volume Metrics
Use the Metrics dashboard to monitor validations, transformations, and user activity by date, user, and operation type.
Key Capabilities
API Capabilities
Built for quality, clinical, and data operations teams preparing for audit and automation:
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Upload CCDs for validation through API
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Automatically trigger transformation workflows
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Retrieve corrected CCDs for ingestion into downstream systems
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Export validation results for internal QA or audit trails
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Query metrics and system usage programmatically
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Trial access includes API keys and documentation.
Security and Trust
We are committed to data safety and compliance.
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No CCDs are stored or persisted after upload
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HTTPS encryption protects all data in transit
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Trial sessions are fully isolated
Important: This is a trial version intended only for evaluation. Do not upload any real patient data. Use synthetic or de-identified CCDs only.
Simplify Your Path to NCQA, HEDIS, and dQM Success
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Identify and correct structural issues that block compliance
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Align with NCQA’s DAV specifications and supplemental data standards
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Prepare CCDs for FHIR mapping, CQL execution, and future dQM initiatives
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Avoid costly PSV efforts by submitting validated documents
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Export clean CCDs with traceable corrections for audit readiness
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Monitor document quality at scale using the built-in Metrics dashboard
Get started instantly — no installation, no setup, no dependencies
Frequently Asked Questions
What document types are supported?
C-CDA documents in .xml format, including CCDs used for quality reporting and supplemental data submission.
How is this tool different from a generic validator?
It is aligned with NCQA expectations, allows auto-transformation of failed documents, and prepares CCDs for DAV and dQM programs.
Is this tool relevant for HEDIS submissions?
Yes. Corrected CCDs can be used as standard supplemental data in HEDIS reporting when submitted through NCQA-validated aggregators.
Can this support the shift to digital measures?
Yes. It ensures your data structure and content are ready for use in FHIR-based digital quality measurement workflows.
Can I use this in a pipeline or integrate it into our tools?
Yes. API endpoints are available for automated validation, transformation, and metrics tracking.
Can I use PHI during the trial?
No. This is a shared trial environment. Please use only synthetic or de-identified data.
Begin Your NCQA Readiness Today
Validate and Transform CCDs for NCQA, HEDIS, and Digital Quality Programs
Deliver cleaner data, reduce audit effort, and future-proof your quality pipeline with automated validation and transformation.
Get Access
Start using the Care Compliance Validator now or connect with our team for scalable implementation support.
(No PHI required. Trial use only.)
Note: NCQA is a registered trademark of the National Committee for Quality Assurance. National Committee for Quality Assurance (NCQA) is not affiliated with or endorsing this product.