IEC 62304:2015 Medical Device Software Lifecycle ProcessesvsICH Q10 - Pharmaceutical Quality System
See exactly how IEC 62304:2015 Medical Device Software Lifecycle Processes controls map to ICH Q10 - Pharmaceutical Quality System. Pre-computed mappings, identified gaps, and coverage analysis.
Need this as a report you can hand to an assessor? A coverage crosswalk for this pair can be built to order.
According to the TheArtOfService Compliance Knowledge Graph:
IEC 62304:2015 Medical Device Software Lifecycle Processes maps to ICH Q10 - Pharmaceutical Quality System with 27% coverage across 9 directly mapped controls. Analysis of 33 IEC 62304:2015 Medical Device Software Lifecycle Processes controls identifies 24 compliance gaps, primarily concentrated in Clause 9 - Software Problem Resolution Process.
Source: TheArtOfService Knowledge Graph | 33 controls analysed | 692 frameworks | 306K+ cross-framework mappings
Control Mappings
Showing 13 of 13 mapped controls across 5 domains. Sign up to explore all 306K+ mappings across 692 frameworks.
Clause 4 - General Requirements(2 mappings)
Clause 5 - Software Development Process(5 mappings)
Clause 7 - Software Risk Management Process(3 mappings)
Clause 8 - Software Configuration Management Process(1 mappings)
Clause 9 - Software Problem Resolution Process(2 mappings)
A IEC 62304:2015 Medical Device Software Lifecycle Processes to ICH Q10 - Pharmaceutical Quality System crosswalk, built to order
The table above lists candidate mappings. A crosswalk answers the narrower question you are probably here for: which ICH Q10 - Pharmaceutical Quality System controls your existing IEC 62304:2015 Medical Device Software Lifecycle Processes work already satisfies, which are real gaps, and the reasoning behind every claim so you can check it. One pair, $299, one time.
This direction has not been through crosswalk review and sign off, so no coverage figure is published for it. Reporting an unreviewed number would be worse than reporting none. It can be built to order at the same price as a pair that is already on the shelf.
If the two frameworks turn out to have too little in common for a crosswalk to help you, we say so and refund it rather than send a number worth nothing.
This direction has not been through crosswalk review and sign off, so no coverage figure is published for it. Reporting an unreviewed number would be worse than reporting none. It can be built to order at the same price as a pair that is already on the shelf.
If the two frameworks turn out to have too little in common for a crosswalk to help you, we say so and refund it rather than send a number worth nothing.
- Every evidenced control, with the reasoning behind it
- Every gap, with what it requires
- Its level of review stated plainly, not a bare number
Why this page shows two different percentages. The 27% in the header counts how many IEC 62304:2015 Medical Device Software Lifecycle Processes controls carry at least one candidate mapping in the graph, before any review. The crosswalk percentage counts something stricter: how many ICH Q10 - Pharmaceutical Quality System controls are actually evidenced, after a pass that argued against each mapping and kept only what survived. They answer different questions and they are not meant to agree.
A crosswalk narrows the work. It does not replace an audit, and your assessor may take a different view on individual controls. Mappings between frameworks are judgements, not text printed in either standard, which is why every claim in the report shows its reasoning. Questions go to support@theartofservice.com.
Related Comparisons
Other IEC 62304:2015 Medical Device Software Lifecycle Processes comparisons
Other ICH Q10 - Pharmaceutical Quality System comparisons
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What are the key differences between IEC 62304:2015 Medical Device Software Lifecycle Processes and ICH Q10 - Pharmaceutical Quality System?
IEC 62304:2015 Medical Device Software Lifecycle Processes has 33 controls across its framework, while ICH Q10 - Pharmaceutical Quality System covers 6 controls. Direct mapping analysis identifies 9 overlapping controls (27% coverage). The frameworks diverge most significantly in Clause 9 - Software Problem Resolution Process, where 6 IEC 62304:2015 Medical Device Software Lifecycle Processes controls have no direct ICH Q10 - Pharmaceutical Quality System equivalent.
How many controls map between IEC 62304:2015 Medical Device Software Lifecycle Processes and ICH Q10 - Pharmaceutical Quality System?
Of 33 total IEC 62304:2015 Medical Device Software Lifecycle Processes controls, 9 map directly to ICH Q10 - Pharmaceutical Quality System controls, representing 27% coverage. The remaining 24 controls represent compliance gaps requiring additional documentation or compensating controls to satisfy both frameworks simultaneously.
What are the compliance gaps when mapping IEC 62304:2015 Medical Device Software Lifecycle Processes to ICH Q10 - Pharmaceutical Quality System?
24 IEC 62304:2015 Medical Device Software Lifecycle Processes controls have no direct equivalent in ICH Q10 - Pharmaceutical Quality System. The highest concentration of gaps is in Clause 9 - Software Problem Resolution Process with 6 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 IEC 62304:2015 Medical Device Software Lifecycle Processes and ICH Q10 - Pharmaceutical Quality System?
The domain with the highest gap count is Clause 9 - Software Problem Resolution Process (6 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.
Related Resources
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