Cross-Framework Mapping

IEC 62304:2015 Medical Device Software Lifecycle ProcessesvsSingapore Cybersecurity Act 2018

See exactly how IEC 62304:2015 Medical Device Software Lifecycle Processes controls map to Singapore Cybersecurity Act 2018. Pre-computed mappings, identified gaps, and coverage analysis.

3
Controls Mapped
30
Gaps Found
9%
Coverage

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 Singapore Cybersecurity Act 2018 with 9% coverage across 3 directly mapped controls. Analysis of 33 IEC 62304:2015 Medical Device Software Lifecycle Processes controls identifies 30 compliance gaps, primarily concentrated in Clause 9 - Software Problem Resolution Process.

Source: TheArtOfService Knowledge Graph | 33 controls analysed | 686 frameworks | 309K+ cross-framework mappings

Control Mappings

Showing 3 of 3 mapped controls across 2 domains. Sign up to explore all 309K+ mappings across 686 frameworks.

Clause 5 - Software Development Process(2 mappings)

IEC62304-5.2Software Requirements Analysis
SCA-S2Interpretation and Definitions
IEC62304-5.3Software Architectural Design
SCA-S2Interpretation and Definitions

Clause 7 - Software Risk Management Process(1 mappings)

IEC62304-7.2Risk Control Measures
SCA-S2Interpretation and Definitions
Coverage crosswalk

A IEC 62304:2015 Medical Device Software Lifecycle Processes to Singapore Cybersecurity Act 2018 crosswalk, built to order

The table above lists candidate mappings. A crosswalk answers the narrower question you are probably here for: which Singapore Cybersecurity Act 2018 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.

IEC 62304:2015 Medical Device Software Lifecycle Processes into Singapore Cybersecurity Act 2018
Not published yet

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.

Singapore Cybersecurity Act 2018 into IEC 62304:2015 Medical Device Software Lifecycle Processes
Not published yet

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.

IEC 62304:2015 Medical Device Software Lifecycle Processes to Singapore Cybersecurity Act 2018 (built to order)
$299
per framework pair, one time
  • 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 9% 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 Singapore Cybersecurity Act 2018 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 Singapore Cybersecurity Act 2018 comparisons

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What are the key differences between IEC 62304:2015 Medical Device Software Lifecycle Processes and Singapore Cybersecurity Act 2018?

IEC 62304:2015 Medical Device Software Lifecycle Processes has 33 controls across its framework, while Singapore Cybersecurity Act 2018 covers 27 controls. Direct mapping analysis identifies 3 overlapping controls (9% coverage). The frameworks diverge most significantly in Clause 9 - Software Problem Resolution Process, where 8 IEC 62304:2015 Medical Device Software Lifecycle Processes controls have no direct Singapore Cybersecurity Act 2018 equivalent.

How many controls map between IEC 62304:2015 Medical Device Software Lifecycle Processes and Singapore Cybersecurity Act 2018?

Of 33 total IEC 62304:2015 Medical Device Software Lifecycle Processes controls, 3 map directly to Singapore Cybersecurity Act 2018 controls, representing 9% coverage. The remaining 30 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 Singapore Cybersecurity Act 2018?

30 IEC 62304:2015 Medical Device Software Lifecycle Processes controls have no direct equivalent in Singapore Cybersecurity Act 2018. The highest concentration of gaps is in Clause 9 - Software Problem Resolution Process with 8 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 Singapore Cybersecurity Act 2018?

The domain with the highest gap count is Clause 9 - Software Problem Resolution Process (8 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.