EU Medical Devices Regulation (MDR 2017/745)vsEU Cyber Resilience Act
See exactly how EU Medical Devices Regulation (MDR 2017/745) controls map to EU Cyber Resilience Act. Pre-computed mappings, identified gaps, and coverage analysis.
According to the TheArtOfService Compliance Knowledge Graph:
EU Medical Devices Regulation (MDR 2017/745) maps to EU Cyber Resilience Act with 4% coverage across 1 directly mapped controls. Analysis of 26 EU Medical Devices Regulation (MDR 2017/745) controls identifies 25 compliance gaps — primarily concentrated in MDR - PMS + Vigilance + Market Surveillance + Final (Ch VII-X).
Source: TheArtOfService Knowledge Graph | 26 controls analysed | 723 frameworks | 332K+ cross-framework mappings
Control Mappings
Showing 1 of 1 mapped controls across 1 domains. Sign up to explore all 332K+ mappings across 723 frameworks.
MDR - PMS + Vigilance + Market Surveillance + Final (Ch VII-X)(1 mappings)
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What are the key differences between EU Medical Devices Regulation (MDR 2017/745) and EU Cyber Resilience Act?
EU Medical Devices Regulation (MDR 2017/745) has 26 controls across its framework, while EU Cyber Resilience Act covers 24 controls. Direct mapping analysis identifies 1 overlapping controls (4% coverage). The frameworks diverge most significantly in MDR - PMS + Vigilance + Market Surveillance + Final (Ch VII-X), where 7 EU Medical Devices Regulation (MDR 2017/745) controls have no direct EU Cyber Resilience Act equivalent.
How many controls map between EU Medical Devices Regulation (MDR 2017/745) and EU Cyber Resilience Act?
Of 26 total EU Medical Devices Regulation (MDR 2017/745) controls, 1 map directly to EU Cyber Resilience Act controls — representing 4% coverage. The remaining 25 controls represent compliance gaps requiring additional documentation or compensating controls to satisfy both frameworks simultaneously.
What are the compliance gaps when mapping EU Medical Devices Regulation (MDR 2017/745) to EU Cyber Resilience Act?
25 EU Medical Devices Regulation (MDR 2017/745) controls have no direct equivalent in EU Cyber Resilience Act. The highest concentration of gaps is in MDR - PMS + Vigilance + Market Surveillance + Final (Ch VII-X) with 7 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 EU Medical Devices Regulation (MDR 2017/745) and EU Cyber Resilience Act?
The domain with the highest gap count is MDR - PMS + Vigilance + Market Surveillance + Final (Ch VII-X) (7 gaps). Export the full domain-by-domain gap breakdown via the Professional tier to generate a prioritised remediation roadmap.
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