Cross-Framework Mapping

ISO 15189:2022 - Medical Laboratories Requirements for Quality and CompetencevsISO/IEC 25012:2008 - Data Quality Model

See exactly how ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls map to ISO/IEC 25012:2008 - Data Quality Model. Pre-computed mappings, identified gaps, and coverage analysis.

16
Controls Mapped
61
Gaps Found
13%
Coverage

According to the TheArtOfService Compliance Knowledge Graph:

ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence maps to ISO/IEC 25012:2008 - Data Quality Model with 13% coverage across 10 directly mapped controls. Analysis of 77 ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls identifies 67 compliance gaps — primarily concentrated in Clause 7: Process Requirements.

Source: TheArtOfService Knowledge Graph | 77 controls analysed | 718 frameworks | 332K+ cross-framework mappings

Control Mappings

Showing 16 of 16 mapped controls across 4 domains. Sign up to explore all 332K+ mappings across 718 frameworks.

Resource Requirements(6 mappings)

6.5Preparing and Distributing Audit Report2 targets
ISO-25012-5.2Defining data quality measures
ISO-25012-5.3Planning and performing data quality evaluations
6.6Confidentiality or non-disclosure agreements2 targets
25012-ConfidentialityConfidentiality
ISO-25012-4.8Confidentiality
6.7Conducting Audit Follow-up2 targets
ISO-25012-5.2Defining data quality measures
ISO-25012-5.3Planning and performing data quality evaluations

Management System(1 mappings)

8.5Control effectiveness review
ISO-25012-4.11Traceability

Clause 5: Structural and Governance Requirements(4 mappings)

ISO-15189-5.1Legal entity2 targets
ISO-25012-5.2Defining data quality measures
ISO-25012-5.3Planning and performing data quality evaluations
ISO-15189-5.4Structure and authority2 targets
ISO-25012-5.2Defining data quality measures
ISO-25012-5.3Planning and performing data quality evaluations

Clause 6: Resource Requirements(5 mappings)

ISO-15189-6.3Facilities and environmental conditions
ISO-25012-4.11Traceability
ISO-15189-6.5Equipment calibration and metrological traceability
ISO-25012-4.11Traceability
ISO-15189-6.7Service agreements2 targets
ISO-25012-5.2Defining data quality measures
ISO-25012-5.3Planning and performing data quality evaluations
ISO-17025-6.5Metrological traceability
ISO-25012-4.11Traceability

Related Comparisons

Other ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence comparisons

Other ISO/IEC 25012:2008 - Data Quality Model comparisons

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What are the key differences between ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence and ISO/IEC 25012:2008 - Data Quality Model?

ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence has 77 controls across its framework, while ISO/IEC 25012:2008 - Data Quality Model covers 36 controls. Direct mapping analysis identifies 10 overlapping controls (13% coverage). The frameworks diverge most significantly in Clause 7: Process Requirements, where 19 ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls have no direct ISO/IEC 25012:2008 - Data Quality Model equivalent.

How many controls map between ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence and ISO/IEC 25012:2008 - Data Quality Model?

Of 77 total ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls, 10 map directly to ISO/IEC 25012:2008 - Data Quality Model controls — representing 13% coverage. The remaining 67 controls represent compliance gaps requiring additional documentation or compensating controls to satisfy both frameworks simultaneously.

What are the compliance gaps when mapping ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence to ISO/IEC 25012:2008 - Data Quality Model?

67 ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls have no direct equivalent in ISO/IEC 25012:2008 - Data Quality Model. The highest concentration of gaps is in Clause 7: Process Requirements with 19 unmapped controls. These gaps represent areas where additional controls, policies, or documentation must be created to achieve compliance with both frameworks.

Which control domains have the most gaps between ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence and ISO/IEC 25012:2008 - Data Quality Model?

The domain with the highest gap count is Clause 7: Process Requirements (19 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.

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