Annex 11 to EU GMP - Computerised SystemsvsIEC 62304:2015 Medical Device Software Lifecycle Processes
See exactly how Annex 11 to EU GMP - Computerised Systems controls map to IEC 62304:2015 Medical Device Software Lifecycle Processes. Pre-computed mappings, identified gaps, and coverage analysis.
According to the TheArtOfService Compliance Knowledge Graph:
Annex 11 to EU GMP - Computerised Systems maps to IEC 62304:2015 Medical Device Software Lifecycle Processes with 24% coverage across 4 directly mapped controls. Analysis of 17 Annex 11 to EU GMP - Computerised Systems controls identifies 13 compliance gaps — primarily concentrated in Operational Phase - Data Management.
Source: TheArtOfService Knowledge Graph | 17 controls analysed | 723 frameworks | 332K+ cross-framework mappings
Control Mappings
Showing 20 of 27 mapped controls across 2 domains. Sign up to explore all 332K+ mappings across 723 frameworks.
General Requirements (Annex 11)(16 mappings)
Operational Phase - Change and Configuration(4 mappings)
+7 more mappings
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Related Comparisons
Other Annex 11 to EU GMP - Computerised Systems comparisons
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What are the key differences between Annex 11 to EU GMP - Computerised Systems and IEC 62304:2015 Medical Device Software Lifecycle Processes?
Annex 11 to EU GMP - Computerised Systems has 17 controls across its framework, while IEC 62304:2015 Medical Device Software Lifecycle Processes covers 33 controls. Direct mapping analysis identifies 4 overlapping controls (24% coverage). The frameworks diverge most significantly in Operational Phase - Data Management, where 5 Annex 11 to EU GMP - Computerised Systems controls have no direct IEC 62304:2015 Medical Device Software Lifecycle Processes equivalent.
How many controls map between Annex 11 to EU GMP - Computerised Systems and IEC 62304:2015 Medical Device Software Lifecycle Processes?
Of 17 total Annex 11 to EU GMP - Computerised Systems controls, 4 map directly to IEC 62304:2015 Medical Device Software Lifecycle Processes controls — representing 24% coverage. The remaining 13 controls represent compliance gaps requiring additional documentation or compensating controls to satisfy both frameworks simultaneously.
What are the compliance gaps when mapping Annex 11 to EU GMP - Computerised Systems to IEC 62304:2015 Medical Device Software Lifecycle Processes?
13 Annex 11 to EU GMP - Computerised Systems controls have no direct equivalent in IEC 62304:2015 Medical Device Software Lifecycle Processes. The highest concentration of gaps is in Operational Phase - Data Management 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 Annex 11 to EU GMP - Computerised Systems and IEC 62304:2015 Medical Device Software Lifecycle Processes?
The domain with the highest gap count is Operational Phase - Data Management (5 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.
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