FDA Quality Management System Regulation (QMSR)vsISO/IEC 27010:2015
See exactly how FDA Quality Management System Regulation (QMSR) controls map to ISO/IEC 27010:2015. Pre-computed mappings, identified gaps, and coverage analysis.
According to the TheArtOfService Compliance Knowledge Graph:
FDA Quality Management System Regulation (QMSR) maps to ISO/IEC 27010:2015 with 15% coverage across 2 directly mapped controls. Analysis of 13 FDA Quality Management System Regulation (QMSR) controls identifies 11 compliance gaps — primarily concentrated in QMSR: Quality Management System Requirements (§820.10 incorporating ISO 13485:2016 Sec. 4-8).
Source: TheArtOfService Knowledge Graph | 13 controls analysed | 718 frameworks | 332K+ cross-framework mappings
Control Mappings
Showing 4 of 4 mapped controls across 2 domains. Sign up to explore all 332K+ mappings across 718 frameworks.
QMSR: Device Labelling and Packaging Controls (§820.45)(2 mappings)
QMSR: Quality Management System Requirements (§820.10 incorporating ISO 13485:2016 Sec. 4-8)(2 mappings)
Related Comparisons
Other FDA Quality Management System Regulation (QMSR) comparisons
Other ISO/IEC 27010:2015 comparisons
Stop Paying Consultants to Read Spreadsheets
AI-powered compliance intelligence across 718 frameworks — at a fraction of consulting costs.
Free
- ✓ 718 framework browser
- ✓ Cross-framework mappings (332K+)
- ✓ 824 compliance assessments
- ✓ 3 AI queries & searches per day
Professional
- ✓ Unlimited AI Compliance Advisory
- ✓ Unlimited full-text search
- ✓ Framework self-assessment
- ✓ PDF, Excel & CSV exports
What are the key differences between FDA Quality Management System Regulation (QMSR) and ISO/IEC 27010:2015?
FDA Quality Management System Regulation (QMSR) has 13 controls across its framework, while ISO/IEC 27010:2015 covers 28 controls. Direct mapping analysis identifies 2 overlapping controls (15% coverage). The frameworks diverge most significantly in QMSR: Quality Management System Requirements (§820.10 incorporating ISO 13485:2016 Sec. 4-8), where 5 FDA Quality Management System Regulation (QMSR) controls have no direct ISO/IEC 27010:2015 equivalent.
How many controls map between FDA Quality Management System Regulation (QMSR) and ISO/IEC 27010:2015?
Of 13 total FDA Quality Management System Regulation (QMSR) controls, 2 map directly to ISO/IEC 27010:2015 controls — representing 15% coverage. The remaining 11 controls represent compliance gaps requiring additional documentation or compensating controls to satisfy both frameworks simultaneously.
What are the compliance gaps when mapping FDA Quality Management System Regulation (QMSR) to ISO/IEC 27010:2015?
11 FDA Quality Management System Regulation (QMSR) controls have no direct equivalent in ISO/IEC 27010:2015. The highest concentration of gaps is in QMSR: Quality Management System Requirements (§820.10 incorporating ISO 13485:2016 Sec. 4-8) with 5 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 FDA Quality Management System Regulation (QMSR) and ISO/IEC 27010:2015?
The domain with the highest gap count is QMSR: Quality Management System Requirements (§820.10 incorporating ISO 13485:2016 Sec. 4-8) (5 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.
Related Resources
This platform provides educational compliance tools, not legal, regulatory, or professional compliance advice. Cross-framework mappings are AI-assisted interpretations and do not reproduce or replace official standards. Framework names and trademarks belong to their respective owners. Consult qualified professionals for your specific compliance requirements. See our Terms of Service.