Cross-Framework Mapping

ISO 15189:2022 - Medical Laboratories Requirements for Quality and CompetencevsISO/IEC 17025:2017 - General Requirements for Testing and Calibration

See exactly how ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls map to ISO/IEC 17025:2017 - General Requirements for Testing and Calibration. Pre-computed mappings, identified gaps, and coverage analysis.

32
Controls Mapped
45
Gaps Found
40%
Coverage

According to the TheArtOfService Compliance Knowledge Graph:

ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence maps to ISO/IEC 17025:2017 - General Requirements for Testing and Calibration with 40% coverage across 31 directly mapped controls. Analysis of 77 ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls identifies 46 compliance gaps — primarily concentrated in Clause 6: Resource Requirements.

Source: TheArtOfService Knowledge Graph | 77 controls analysed | 723 frameworks | 332K+ cross-framework mappings

Control Mappings

Showing 20 of 32 mapped controls across 5 domains. Sign up to explore all 332K+ mappings across 723 frameworks.

Resource Requirements(2 mappings)

6.6Confidentiality or non-disclosure agreements
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::4.2Confidentiality
6.8Externally Provided Products and Services
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::6.6Externally provided products and services

Management System(1 mappings)

8.9Management Reviews
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::8.9Management reviews (Option A)

Clause 6: Resource Requirements(5 mappings)

ISO-15189-6.3Facilities and environmental conditions
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::6.3Facilities and environmental conditions
ISO-15189-6.8Externally provided products and services
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::6.6Externally provided products and services
ISO-17025-6.3Facilities and environmental conditions
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::6.3Facilities and environmental conditions
ISO-17025-6.5Metrological traceability
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::6.5Metrological traceability
ISO-17025-6.6Externally provided products and services
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::6.6Externally provided products and services

Clause 7: Process Requirements(12 mappings)

ISO-15189-7.5Nonconforming work
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.10Nonconforming work
ISO-15189-7.6Data and information management
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.11Control of data and information management
ISO-17025-7.1Review of requests, tenders and contracts
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.1Review of requests, tenders and contracts
ISO-17025-7.10Nonconforming work
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.10Nonconforming work
ISO-17025-7.11Control of data and information management
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.11Control of data and information management
ISO-17025-7.2Selection, verification and validation of methods2 targets
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.2Selection, verification and validation of methods
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.2.1Selection and verification of methods
ISO-17025-7.4Handling of test or calibration items
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.4Handling of test or calibration items
ISO-17025-7.5Technical records
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.5Technical records
ISO-17025-7.6Evaluation of measurement uncertainty
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.6Evaluation of measurement uncertainty
ISO-17025-7.7Ensuring the validity of results
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.7Ensuring the validity of results
ISO-17025-7.8Reporting of results
iso-iec-17025-2017-general-requirements-for-testing-and-calibration::7.8Reporting of results

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Related Comparisons

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

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What are the key differences between ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence and ISO/IEC 17025:2017 - General Requirements for Testing and Calibration?

ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence has 77 controls across its framework, while ISO/IEC 17025:2017 - General Requirements for Testing and Calibration covers 41 controls. Direct mapping analysis identifies 31 overlapping controls (40% coverage). The frameworks diverge most significantly in Clause 6: Resource Requirements, where 11 ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls have no direct ISO/IEC 17025:2017 - General Requirements for Testing and Calibration equivalent.

How many controls map between ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence and ISO/IEC 17025:2017 - General Requirements for Testing and Calibration?

Of 77 total ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls, 31 map directly to ISO/IEC 17025:2017 - General Requirements for Testing and Calibration controls — representing 40% coverage. The remaining 46 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 17025:2017 - General Requirements for Testing and Calibration?

46 ISO 15189:2022 - Medical Laboratories Requirements for Quality and Competence controls have no direct equivalent in ISO/IEC 17025:2017 - General Requirements for Testing and Calibration. The highest concentration of gaps is in Clause 6: Resource Requirements with 11 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 17025:2017 - General Requirements for Testing and Calibration?

The domain with the highest gap count is Clause 6: Resource Requirements (11 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.

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