Plan, document, and control the design and development process per ISO 9001 Section 8.3 supplemented by AQAP 2110 Edition D requirements. Establish design inputs (regulatory + statutory + customer + reliability + maintainability + safety) and design outputs (drawings + specifications + verification criteria + acceptance criteria + production traveler). Conduct formal design reviews, design verification, design validation, and design transfer including ISO 13485 Clause 7.3.1-7.3.9 cross-walk for medical-device-adjacent defence systems. Maintain dependability requirements (reliability + maintainability + availability + safety + security).
The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.