Cross-Framework Mapping

ISO 15189:2022 — Medical Laboratories Requirements for Quality and CompetencevsICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems

See exactly how ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence controls map to ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems. Pre-computed mappings, identified gaps, and coverage analysis.

18
Controls Mapped
46
Gaps Found
14%
Coverage

According to the TheArtOfService Compliance Knowledge Graph:

ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence maps to ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems with 14% coverage across 9 directly mapped controls. Analysis of 64 ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence controls identifies 55 compliance gaps — primarily concentrated in Clause 7: Process Requirements.

Source: TheArtOfService Knowledge Graph | 64 controls analysed | 693 frameworks | 819K+ cross-framework mappings

Control Mappings

Showing 18 of 18 mapped controls across 4 domains. Sign up to explore all 819K+ mappings across 693 frameworks.

Clause 5: Structural and Governance Requirements(5 mappings)

ISO-15189-5.1Legal entity
E6R2-1.1Glossary and Definitions
ISO-15189-5.4Structure and authority
E6R2-1.1Glossary and Definitions
ISO-15189-5.6Risk management3 targets
E6R2-8.1Before Clinical Phase Commences
E6R2-8.2During Clinical Conduct
E6R2-8.3After Completion or Termination

Clause 6: Resource Requirements(1 mappings)

ISO-15189-6.7Service agreements
E6R2-1.1Glossary and Definitions

Clause 7: Process Requirements(3 mappings)

ISO-15189-7.4Post-examination processes3 targets
E6R2-8.1Before Clinical Phase Commences
E6R2-8.2During Clinical Conduct
E6R2-8.3After Completion or Termination

Clause 8: Management System Requirements(9 mappings)

ISO-15189-8.1General requirements2 targets
E6R2-2.13Quality Management Systems
E6R2-5.0Quality Management
ISO-15189-8.4Control of records3 targets
E6R2-8.1Before Clinical Phase Commences
E6R2-8.2During Clinical Conduct
E6R2-8.3After Completion or Termination
ISO-17025-8.1Options2 targets
E6R2-2.13Quality Management Systems
E6R2-5.0Quality Management
ISO-17025-8.7Corrective actions2 targets
E6R2-2.13Quality Management Systems
E6R2-5.0Quality Management

Related Comparisons

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

Other ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems comparisons

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What are the key differences between ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence and ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems?

ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence has 64 controls across its framework, while ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems covers 22 controls. Direct mapping analysis identifies 9 overlapping controls (14% coverage). The frameworks diverge most significantly in Clause 7: Process Requirements, where 18 ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence controls have no direct ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems equivalent.

How many controls map between ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence and ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems?

Of 64 total ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence controls, 9 map directly to ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems controls — representing 14% coverage. The remaining 55 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 ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems?

55 ISO 15189:2022 — Medical Laboratories Requirements for Quality and Competence controls have no direct equivalent in ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems. The highest concentration of gaps is in Clause 7: Process Requirements with 18 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 ICH E6(R2) Good Clinical Practice — Data Integrity and Electronic Systems?

The domain with the highest gap count is Clause 7: Process Requirements (18 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.

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