Cross-Framework Mapping

FDA Quality Management System Regulation (QMSR)vsGAMP 5 - Good Automated Manufacturing Practice

See exactly how FDA Quality Management System Regulation (QMSR) controls map to GAMP 5 - Good Automated Manufacturing Practice. Pre-computed mappings, identified gaps, and coverage analysis.

5
Controls Mapped
8
Gaps Found
31%
Coverage

According to the TheArtOfService Compliance Knowledge Graph:

FDA Quality Management System Regulation (QMSR) maps to GAMP 5 - Good Automated Manufacturing Practice with 31% coverage across 4 directly mapped controls. Analysis of 13 FDA Quality Management System Regulation (QMSR) controls identifies 9 compliance gaps — primarily concentrated in QMSR: Transition Plan from Prior QSR, FDA Inspection Approach, Status.

Source: TheArtOfService Knowledge Graph | 13 controls analysed | 718 frameworks | 332K+ cross-framework mappings

Control Mappings

Showing 5 of 5 mapped controls across 1 domains. Sign up to explore all 332K+ mappings across 718 frameworks.

QMSR: Quality Management System Requirements (§820.10 incorporating ISO 13485:2016 Sec. 4-8)(5 mappings)

QMSR-820.10Requirements for a Quality Management System - ISO 13485:2016 Sections 4-8 incorporation (§820.10)
GAMP5-Risk-CriticalThinkingRisk-Based Approach, Critical Thinking and 5 Key Concepts
QMSR-ISO13485-Sec5Management responsibility (ISO 13485:2016 Section 5 - incorporated via §820.10)2 targets
GAMP5-Lifecycle-VModel-URS-FS-DS-IQOQPQV-Model Lifecycle - URS + FS + DS + IQ + OQ + PQ + Traceability
GAMP5-Risk-CriticalThinkingRisk-Based Approach, Critical Thinking and 5 Key Concepts
QMSR-ISO13485-Sec7_DesignControlsProduct realization - Design and Development controls (ISO 13485:2016 Section 7.3)
GAMP5-Risk-CriticalThinkingRisk-Based Approach, Critical Thinking and 5 Key Concepts
QMSR-ISO13485-Sec7_PurchasingPurchasing controls + supplier management (ISO 13485:2016 Section 7.4)
GAMP5-2nd-Edition-AI-Cloud-Agile-CSA2nd Edition (2022) - AI/ML, Cloud, Agile, DevOps and Computer Software Assurance (CSA)

Related Comparisons

Other FDA Quality Management System Regulation (QMSR) comparisons

Other GAMP 5 - Good Automated Manufacturing Practice comparisons

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What are the key differences between FDA Quality Management System Regulation (QMSR) and GAMP 5 - Good Automated Manufacturing Practice?

FDA Quality Management System Regulation (QMSR) has 13 controls across its framework, while GAMP 5 - Good Automated Manufacturing Practice covers 11 controls. Direct mapping analysis identifies 4 overlapping controls (31% coverage). The frameworks diverge most significantly in QMSR: Transition Plan from Prior QSR, FDA Inspection Approach, Status, where 2 FDA Quality Management System Regulation (QMSR) controls have no direct GAMP 5 - Good Automated Manufacturing Practice equivalent.

How many controls map between FDA Quality Management System Regulation (QMSR) and GAMP 5 - Good Automated Manufacturing Practice?

Of 13 total FDA Quality Management System Regulation (QMSR) controls, 4 map directly to GAMP 5 - Good Automated Manufacturing Practice controls — representing 31% coverage. The remaining 9 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 GAMP 5 - Good Automated Manufacturing Practice?

9 FDA Quality Management System Regulation (QMSR) controls have no direct equivalent in GAMP 5 - Good Automated Manufacturing Practice. The highest concentration of gaps is in QMSR: Transition Plan from Prior QSR, FDA Inspection Approach, Status with 2 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 GAMP 5 - Good Automated Manufacturing Practice?

The domain with the highest gap count is QMSR: Transition Plan from Prior QSR, FDA Inspection Approach, Status (2 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.

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.