Equipment qualification
Laboratory procedures for temperature, altitude, vibration, fluids, power input, RF susceptibility and emissions, lightning, electrostatic discharge, icing, and other installed environments.
FAA AC 21-16G ↗AIRWORTHINESS · DEVELOPMENT ASSURANCE · COMPLIANCE
A field guide to the approval path for aircraft, systems, software, airborne electronic hardware, tools, and equipment qualification. Start with the certification basis and safety assessment; use standards as coordinated means of compliance.
EDUCATIONAL REFERENCE · REFERENCE UPDATED OCTOBER 5, 2026A standard is not the certificate. The FAA approves a product or article against an agreed certification basis. Advisory circulars describe accepted approaches, but applicants must coordinate the specific means of compliance, plans, data, reviews, tests, and findings for their project.
CERTIFICATION ROADMAP
Familiarize the FAA with the product, intended use, novel features, organization, and certification request.
Establish the certification basis, applicable regulations, special conditions, exemptions, and equivalent-safety findings.
Agree on certification plans, means of compliance, schedules, delegation, conformity, and authority involvement.
Develop the design and production-quality system under configuration, supplier, and conformity controls.
Complete analyses, inspections, laboratory and ground testing, flight testing, and compliance findings.
Close issues and open problem reports, finalize approved data and manuals, and obtain the design approval.
Show repeatable conformity to the approved design and sustain continued operational safety after entry into service.
Roadmap aligned with the FAA’s 2026 seven-phase aircraft certification overview. A TSO authorization, STC, PMA, or other approval follows a path tailored to its regulatory purpose.
CORE STANDARDS
Laboratory procedures for temperature, altitude, vibration, fluids, power input, RF susceptibility and emissions, lightning, electrostatic discharge, icing, and other installed environments.
FAA AC 21-16G ↗Life-cycle objectives for planning, development, verification, configuration management, quality assurance, and certification liaison. Software level A through E follows the system safety classification.
FAA AC 20-115D ↗Design assurance for complex custom devices and associated hardware evidence, including planning, requirements capture, detailed design, implementation, validation, verification, and process assurance.
FAA AC 20-152A ↗Qualification objectives for tools whose output is relied upon without the verification that would otherwise detect an error, or that could fail to detect an error. Scope qualification to the claimed use and tool qualification level.
RTCA software standards ↗Coordinates requirements, architecture, allocation, validation, verification, integration, and development assurance. FAA AC 20-174 currently recognizes ARP4754A; coordinate use of the newer ARP4754B with the FAA for the specific project.
FAA AC 20-174 ↗Methods supporting functional hazard assessment, preliminary and final system safety assessment, common-cause analysis, fault trees, FMEA, and quantitative or qualitative safety objectives.
FAA AC 25.1309-1B ↗HOW THE PIECES CONNECT
Do not choose DO-178C or DO-254 levels by intuition. Classify aircraft and system failure conditions, allocate safety requirements, then flow the resulting assurance rigor to software and hardware items.
SUPPORTING GUIDANCE
Supplement to DO-178C for executable models and model-based verification.
Addresses object-oriented and related techniques used in airborne software.
Defines how formal methods may satisfy or modify selected DO-178C objectives.
Roles, artifacts, and assurance for shared IMA platforms, applications, and integration.
Data-quality processes for navigation and other installed aeronautical databases.
Security process and methods for intentional unauthorized electronic interaction and connected aircraft systems.
FAA guidance for managing unresolved system, software, and hardware problem reports at approval.
Address workload, controls, displays, alerts, foreseeable misuse, maintainability, and operational limitations early.
PROGRAM ADVICE
ONE-STOP REFERENCE
Find a document, its purpose and a practical place to manage it. These are reference names and recommended workflows, not a prescribed company data list. The approved plans define the actual titles, contents, owners and release process.
21 document entries
| Acronym / full title | Family | Typical home / export | Purpose & naming notes |
|---|---|---|---|
| PSAC / PHACPlan for Software / Hardware Aspects of Certification | Planning | Word → controlled PDF | Defines the item, assurance level, life cycle, compliance approach, data, suppliers, tools, and authority coordination. PHAC describes how the applicant will develop and substantiate the hardware functions for the identified product. |
| SDP / HDPSoftware Development Plan / Hardware Design Plan | Planning | Word → controlled PDF | Organizes development activities, responsibilities, standards, design methods and transitions. “Hardware Development Plan” is also a local title; DO-254 uses Hardware Design Plan. |
| SVP / HVPSoftware / Hardware Verification Plan | Planning | Word → controlled PDF | Defines verification methods, independence, environments, coverage and completion criteria. HVP alone does not necessarily cover requirements validation. |
| HVVPHardware Validation and Verification Plan | Planning | Word → controlled PDF | Common combined plan: validation asks whether requirements are correct and complete; verification asks whether implementation meets them. Document the two activities distinctly. |
| SCMP / HCMPSoftware / Hardware Configuration Management Plan | Planning | Word → controlled PDF | Defines identification, baselines, change control, problem reporting, release and archival controls. |
| SQAP / HQAPSoftware / Hardware Quality Assurance Plan | Planning | Word → controlled PDF | HQAP ends in “Assurance Plan,” not just “Hardware Quality.” Explain its relationship to DO-254 hardware process assurance; use HPAP when that is the project’s plan title. |
| HPAPHardware Process Assurance Plan | Planning | Word → controlled PDF | Defines independent process oversight, audits, records, deviations and corrective-action closure. Can be coordinated with HQAP. |
| HRS / HDSHardware Requirements Standards / Hardware Design Standards | Planning | Word or controlled standards repository | Defines writing and design conventions; link compliance checks to reviews. Acronyms and packaging vary. |
| HRDHardware Requirements Data / Document | Development | DOORS / DOORS Next → reviewed export | Typical requirements module: unique IDs, allocation, derived requirements, interfaces, rationale, validation status and trace links. “Document” is a common local title. |
| HDDHardware Design Data / Document | Development | DOORS / DOORS Next + design repository | Describe architecture and design decisions in modules where useful. Schematics, HDL, models and implementation files remain controlled in their engineering repositories. |
| HCDProject-specific title: confirm locally | Development | DOORS / DOORS Next if defined by project | May mean Hardware Conceptual Design or Hardware Configuration Data. Use the project glossary to resolve the title. Define it in the PHAC/data-item list before using it. |
| HVTCHardware Verification Test Cases | Verification | DOORS / DOORS Next or ETM | Common local title. Captures test purpose, requirements, inputs, expected outputs, tolerances and pass/fail criteria. Link each case to the requirements it verifies. |
| HVTPHardware Verification Test Procedures (or Test Plan) | Verification | Procedures: DOORS / DOORS Next or ETM; plan: Word/PDF | Ambiguous local acronym. In a DOORS-based verification set, the title may refer to procedures; confirm the template. Procedures give executable steps; a plan sets the strategy. |
| HVTRHardware Verification Test Results / Report | Verification | ETM or results repository → linked DOORS evidence | Common local title. Preserve actual versus expected results, test configuration, execution records, anomalies and review approval. A DOORS export may summarize results; retain the underlying logs. |
| HTDHardware Traceability Data | Verification | DOORS / DOORS Next → controlled report | Common title for bidirectional links across requirements, design and verification evidence, plus unresolved gaps and justified exceptions. |
| HCI / SCIHardware / Software Configuration Index | Completion | Configuration repository → controlled Word/PDF | Identifies the released item and associated life-cycle data revisions. HCI identifies the hardware baseline; SCI identifies the software baseline. |
| HECI / SECIHardware / Software Environment Configuration Index | Completion | Tool/build repository → controlled Word/PDF | Identifies the environment needed to reproduce development and verification. For HECI include relevant workstations/OS, design and verification tools, versions/settings and qualification references; reference it from HCI. |
| HAS / SASHardware / Software Accomplishment Summary | Completion | Word → controlled PDF | Summarizes completed activities, compliance, deviations, approved configuration and outstanding issues for the approval package. |
| HPARHardware Process Assurance Records | Completion | Quality repository → controlled reports | Common expansion; some companies title an individual document “Report.” Keep audit results, nonconformances, corrective actions and closure evidence. Confirm the exact local title. |
| PR / OPRProblem Report / Open Problem Report | Completion | Issue tracker → baseline-linked report | Records defects, impact, disposition and closure. Evaluate open reports against safety, intended function and certification impact; see AC 20-189. |
| TQP / TASTool Qualification Plan / Tool Accomplishment Summary | Tools | Word/PDF + controlled tool evidence | DO-330 software-tool qualification data when applicable. Do not assume DO-330 replaces the DO-254 tool assessment approach; agree the hardware tool approach with the authority. |
No matching documents. Try another term or select all families.
DOORS / DOORS NEXT
Documents do not automatically “come from DOORS.” The project chooses its source of truth. HRD and traceability are natural requirements-tool artifacts. HDD and HCD can be modules with links to engineering files. HVTC and HVTP procedures can be modules or linked test artifacts; HVTR usually combines controlled execution evidence with a reviewed report.
Use controlled Word/PDF for PHAC, PSAC, development/verification/CM/assurance plans, indexes and accomplishment summaries. Link them to module baselines and data-item revisions.
Use DOORS or DOORS Next for structured IDs, attributes, reviews and trace links. Keep HDL, schematics, constraints and build outputs in their controlled design repositories.
With IBM ELM, test cases, scripts and execution records can live in ETM and link to DOORS Next requirements. Classic DOORS workflows may use modules and integrations. Preserve original evidence.
Baseline modules and linked configurations. Export reviewed data with IDs and versions, reconcile trace gaps, and verify that the delivered report matches the approved source baseline.
Source: IBM: linking requirements, design and test artifacts ↗. The workflow recommendations above are practical organization choices; neither the FAA nor DO-254 mandates Word or an IBM product.
EXAMPLE · ONE FPGA REQUIREMENT
HRD-042 → HDD clock/reset design and controlled HDL revision → HVTC-019 / HVTP-019 → HVTR execution evidence → anomaly disposition → HCI release baseline. HECI identifies the tools and environment; HAS summarizes completion. Real IDs and link types follow your project’s process.
A green trace link is not proof of compliance: verify the linked artifact, review status, revision and actual result.Hardware environment and release-index guidance: FAA AC 00-72, §3.1.1 ↗. Hardware verification strategy: FAA AC 20-152A ↗.
STAGES OF INVOLVEMENT
SOI reviews are certification authority or authorized representative reviews of the project’s processes and evidence. Often called “audits,” they combine discussion, data sampling, demonstrations and follow-up actions. The familiar four-stage framework below is a preparation aid; coordinate scope, timing, delegation and readiness criteria with the responsible authority.
Can this approach satisfy the applicable objectives?
Baseline PSAC/PHAC and supporting plans, standards, level rationale, responsibility/independence matrix, tool strategy, supplier approach and proposed review schedule.
Walk reviewers through the intended life cycle. Resolve plan gaps and record agreed actions before the project depends on an unaccepted approach.
Are the plans being followed and is the design traceable?
Representative reviewed requirements, architecture/design, implementation data, derived requirements, traceability, CM records and process-assurance evidence.
Demonstrate requirements-to-design links and change control. For FPGA hardware, include HDL, interfaces, constraints, clock/reset design and implementation evidence as applicable.
Does the evidence show the implemented item meets its requirements?
Reviewed cases/procedures/results, coverage and analyses, reproducible test configuration, independence evidence, anomaly reports and tool-credit rationale.
Follow a requirement through the case, execution and result. Explain uncovered requirements, failures, retests and open issues using the controlled baseline.
Is the certification data package complete and internally consistent?
HAS/SAS, HCI/SCI and environment indexes, final trace/coverage status, assurance records, deviations, open-report assessments and review-action closure.
Show the final release identity and evidence completeness. Close findings or document authority-agreed dispositions; a completed review is not itself a certificate.
Authoritative review guidance: FAA Order 8110.49A, Chapter 2 ↗ and FAA Order 8110.105B, Chapter 2 ↗. Use the licensed DO-178C / DO-254 standards for the applicable objectives and life-cycle data contents.
OFFICIAL STARTING POINTS