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Reconstructed reference notes on EASA acceptable means of compliance for airborne software and airborne electronic hardware, built from AMC 20-115D (ED Decision 2017/020/R, AMC-20 Amendment 14, consolidated in Amendment 23) and AMC 20-152A (ED Decision 2020/010/R, AMC-20 Amendment 19, consolidated in Amendment 23), read from the Easy Access Rules AMC-20 compilation (Amendment 23, June 2023) and pinned 2026-09-26. Use for EASA software means of compliance, EASA AEH means of compliance, AltMoC, ETSO software, and the joint software and hardware certification workflow. SCOPE LIMITS: the two AMC sections only; no FAA content (use faa-8110-49); no RTCA DO-178C or DO-254, EUROCAE ED-12C or ED-80, or supplement clause text (use avionics-signpost to name them); no Part-21 body; no bulk AMC-20; AMC 20-193 and AMC 20-189 are name-only; reflects Amendment 23 as consolidated in the June 2023 EAR, not a later AMC-20 amendment; synthesized reference notes, not legal advice and not the official AMC. LICENCE: per-document (E
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- faa-8110-49jgsystemsconsulting/jgs-se-knowledge-packsReconstructed reference notes on US FAA approval guidance for airborne software and airborne electronic hardware, built from four public-domain sources (FAA Order 8110.49A, AC 20-115D, AC 20-152A, AC 00-69; documents dated 2017-07-21 to 2022-10-07, pinned 2026-10-12). Use for how FAA certification staff plan and conduct software reviews (certification liaison, desk versus on-site review, review planning agreements), how the level of FAA involvement (LOI) is picked and scored with the Appendix A worksheets, how software conformity inspection works (software part and installation conformity, ASE and ASI tasks, Form 8120-10), what AC 20-115D recognizes and how DO-178B processes and tool qualification transition to DO-178C/DO-330 (supplements, FLS, UMS, legacy software changes), and what AC 20-152A adds for airborne electronic hardware (simple versus complex custom devices, robustness and HDL code coverage, tool assessment, previously developed hardware, COTS IP, COTS devices, circuit board assemblies), and what Planificare★ 98
- avionics-signpostjgsystemsconsulting/jgs-se-knowledge-packsSignpost (not a knowledge pack) for the avionics development assurance standards landscape: RTCA DO-178C / EUROCAE ED-12C and its supplements (DO-330/ED-215, DO-331/ED-218, DO-332/ED-217, DO-333/ED-216); RTCA DO-254 / EUROCAE ED-80; SAE ARP4754B and ARP4761A; and the free regulator documents that recognise them (FAA AC 20-115D, AC 20-152A, Order 8110.49A; EASA AMC 20-115D and AMC 20-152A). Contains no source content: each row carries only the designation, title, edition, owner, redistributability status, and the owner's URL. Use when you need to identify, cite, or locate an avionics standard; paywalled rows point to the owner, free rows point to the regulator text, and the FAA rows also name the in-repo faa-8110-49 pack.Juridic★ 98
- med-device-eujgsystemsconsulting/jgs-se-knowledge-packsReconstructed reference notes on EU and UK medical-device software, built from six sources captured 2026-10-13: MDCG 2019-11 rev.1 (June 2025), MDCG 2020-6 (April 2020), MDCG 2020-13 (July 2020), MDCG 2020-7 (April 2020), MDCG 2020-8 (April 2020), and the MHRA software-applications guidance (2023-07-01) with its stand-alone software PDF. Use for SaMD qualification and classification, legacy-device clinical evidence, the clinical evaluation assessment report, the PMCF plan, and the PMCF evaluation report, under EU MDCG guidance or UK MHRA guidance. SCOPE LIMITS: EU MDR and UK MHRA device software only; no IEC 62304, ISO 13485, or ISO 14971 text; no MDR or IVDR regulation body text; MDCG guidance is not legally binding; MHRA guidance is UK-specific; synthesized notes, not legal advice. LICENCE: Per-document: European Commission reuse policy (Decision 2011/833/EU, CC BY 4.0, attribution and indication of changes) for the MDCG documents; Open Government Licence v3.0 for the MHRA guidance; reconstructed notes withDocumente★ 98
- fda-med-devicejgsystemsconsulting/jgs-se-knowledge-packsReconstructed reference notes on US FDA medical-device software regulation, built from seven public-domain FDA sources (the QMSR final rule 89 FR 7496, FDA device software guidance documents, and the eSTAR program page; pinned 2026-10-12). Use for regulatory pathways and premarket submissions (510(k), De Novo, PMA, eSTAR), premarket software documentation levels (Basic or Enhanced), software validation and Computer Software Assurance, the Quality Management System Regulation (QMSR, 21 CFR 820), medical-device cybersecurity (secure product development, SBOMs, FD&C Act section 524B, labelling), clinical decision support boundaries, off-the-shelf software, MDDS and other software-function scope questions, and the 510(k) software-change trigger. SCOPE LIMITS: US FDA device regulation only; no EU MDR or UKCA content (see `med-device-eu`); no ISO 13485, ISO 14971, or IEC 62304 text, which are named and summarized only as FDA obligations; no drug, biologic, or combination-product rules; reflects the pinned source daȘtiință★ 98
- faa-rmajgsystemsconsulting/jgs-se-knowledge-packsKnowledge base from FAA-HDBK-006D (2020), the FAA's System Reliability, Maintainability, and Availability (RMA) Handbook for National Airspace System (NAS) hardware and software. Use for RMA figures of merit (MTBF, MTBO, MTTR, the availability variants), the bathtub curve and probability distributions, the four-stage RMA lifecycle mapped to the FAA Acquisition Management System (AMS), the six-task RMA technical-management/acquisition process, service-thread criticality and the NAS-RD severity-to-target table, the RMA analysis toolbox (RBD, FMEA/FMECA, FTA, Ishikawa, Monte Carlo, Bayesian, FRACAS, ALT, reliability-growth/recovery tests), software reliability (early prediction + reliability growth), and tailorable example RMA requirements for a Program Requirements Document. Scope limits: it is FAA/NAS-specific guidance (not a requirement, by its own statement), centred on hardware-plus-software availability — it brackets out human/service/facility/communications availability, names but does not reproduce the mTestare★ 98
- dod-mosajgsystemsconsulting/jgs-se-knowledge-packsKnowledge base from the OUSD(R&E) guidebook Implementing a MOSA in DoD Programs (Feb 2025). Use for the Modular Open Systems Approach as a DoD acquisition + design discipline: the statutory/regulatory basis (10 U.S.C. 4401–4403, FY2017/FY2021 NDAA, DFARS), the five OUSD(R&E) pillars, the plan→modularize→identify→define→standardize interface lifecycle, technical levers (WBS/MIL-STD-881F taxonomy, standards profiling, API-first software, COTS/cybersecurity), MOSA assessment metrics and tools (PART/OAAT/KOSS/SEAM/MAUT), technology-change and DMSMS management, roadmaps, MOSA across the six AAF pathways, and contracting/IP/data-rights mechanics. SCOPE LIMITS: this is U.S. DoD weapon-system acquisition policy, not a general open-architecture or interface-standards reference — it names standards (FACE, OMS, DISR) without reproducing them, is light on detailed engineering of any specific standard, and does not cover the underlying SE processes (use dau-se-guidebook / nasa-npr-7123) or general systems-engineering theoDesign★ 98
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