Qualityze

QUALITY MANAGEMENT FOR REGULATED INDUSTRIES

Quality Management Software for Aerospace and Defense Industry

Manage AS9100 compliance, FAI, CAPA, configuration control, supplier quality, traceability, and nonconformances with greater control and visibility. Qualityze helps Aerospace & Defense manufacturers connect product, supplier, quality, and compliance processes in one closed-loop QMS.

  • 21 CFR Part 11/EU GMP Annex 11 Ready
  • Risk Based Validation
  • Salesforce-Native Architecture
  • Salesforce
QMS for Aerospace and Defence Industry
  • LifeMD
  • Highridge
  • The Andersons
  • Prayon
  • Grynova Consulting Group
  • Cavin Care

Trusted by quality teams across regulated industries

Read their success stories

INDUSTRY-SPECIFIC CHALLENGES

Aerospace & Defense Challenges, Solved

Qualityze helps Aerospace & Defense manufacturers address quality, compliance, and operational challenges by connecting people, processes, and quality data.

The challenge

Managing changes for drawings, specifications, BOMs, SOPs, suppliers, & product configurations become difficult as programs evolve. Poorly controlled changes can lead to differences between engineering and manufacturing.

How Qualityze solves it

Qualityze QMS for Aerospace and Defense helps teams handle all the critical changes through controlled, closed-loop workflows and linked training programs so every change is traceable and understood by the teams.

SYSTEM CAPABILITIES

How Qualityze Strengthen Aerospace & Defense Quality?

Qualityze QMS software for Aerospace & Defense helps teams standardize quality processes, strengthen supplier controls, and ensure compliance.

Connected, Closed-Loop Platform

Bring engineering changes, inspection records, supplier quality data, nonconformances, CAPAs, and audits in one connected, closed-loop system.

IdentifyTriageAssessInvestigateActVerifyLearn

The system maintains end-to-end traceability for informed decisions.

Connected Aerospace and Defense quality and supplier operations
Connected Aerospace and Defense quality and supplier operations

Enterprise Quality Management System

Manage deviations, nonconformances, specification issues, contamination events, product holds, and CAPAs using standardized workflows.

Connected Aerospace and Defense quality and supplier operations

Product Data Management System

Manage aerospace-controlled product specifications, drawings, BOMs, engineering data, inspection requirements, and revision histories in one secure, validated platform.

Connected Aerospace and Defense quality and supplier operations

Asset Management System

Keep a log of calibration and maintenance status of the gauges, inspection equipment, test systems, tooling, and other critical manufacturing assets.

Connected Aerospace and Defense quality and supplier operations

Environmental, Health and Safety System

Manage environmental and workplace events that can affect aerospace manufacturing, like hazardous materials, FOD events, and more.

Supplier Relationship Management System

Establish stronger quality controls over incoming raw materials, ingredients, SCARs for suppliers and sub tier providers.

QualifyApproveReceiveMonitorChangeCorrect
Connected Aerospace and Defense quality and supplier operations

Post-Market Surveillance Management System

Manage post-market events by linking complaints, product failures, service issues, suppliers, serial numbers and corrective actions.

CaptureAssessInvestigateActTrendImprove
Connected Aerospace and Defense quality and supplier operations

Built-In Continuous Improvement Tools

Use built-in, structured root cause analysis tools like 5Whys, Six Sigma, FMEA and CAPA effectiveness reviews to investigate quality escapes and tighten process controls.

DetectAnalyzePrioritizeCorrectVerifyStandardize
Connected Aerospace and Defense quality and supplier operations

7

Quality, safety, product, asset, supplier, field quality, and improvement management

1

Consistent information across connected records and workflows

100%

Linked actions, approvals, changes, and supporting evidence

Enterprise Visibility

Cross-site insights across teams, processes, and operations

THE SHIFT

From Reactive Quality to Proactive Control

See how Qualityze Aerospace Quality Management Software replaces common compliance bottlenecks with connected, traceable workflows.

Manual and disconnected Aerospace and Defense quality operations

Manual · Fragmented · Risk-Prone

Disconnected engineering changes, drawing revisions, specifications, and work instructions increase configuration risk.
Lack of visibility as supplier defects, SCARs, certifications, audits, and sub-tier quality issues are managed in silos.
Nonconformances and quality escapes can require manual investigation across lots, inspections, and affected assemblies.
First Article Inspection records, inspection results, engineering revisions, and supporting evidence can become difficult to coordinate across teams and suppliers.
Tracking special-process issues, key-characteristic failures, and process risks separately makes recurring quality signals harder to detect.
Controlled and proactive Aerospace and Defense quality operations

Controlled · Connected · Inspection-Ready

Connected change requests with impact assessments, training, and implementation controls to maintain configuration integrity.
Mange supplier qualification, audits, nonconformances, SCARs, and performance data in one closed-loop workflow.
Route nonconformances through containment, investigation, RCA, disposition, CAPA, and effectiveness checks.
Connect inspection records, quality events, approvals, controlled documents, and corrective actions to strengthen verification and production readiness.
Q analyzes historical data for the failure events, process risks, and other failures to detect the recurring issues and investigate them.

Regulatory Frameworks Qualityze Supports

  • AS9100D

    Energy Management System Standards to Optimize Energy Efficiency

  • AS9102 First Article Inspection

    Provides evidence that all the requirements for design, manufacturing, and engineering are understood before producing mass products for aerospace.

  • AS9145 APQP & PPAP

    Definess the APQP and PPAP requirements for Aerospace components and product suppliers so they can proactively manage risks.

  • AS9103 Key Characteristics & Variation Management

    Defines requirements to manage key characteristics and variations that can impact the product conformity and reliability.

  • FAA 14 CFR Part 21

    Defines the rules for getting and maintaining official approvals on aerospace and defense products and related components.

  • Nadcap Special Process Requirements

    Rigorous industry best practices used to evaluate the manufacturing processes that are not part of routine aerospace product inspections.

  • DFARS Counterfeit Electronic Part Prevention Requirements

    Defines a formal process to identify and avoid fake or inappropriate electronic components to be used in Aerospace and Defense products.

  • NIST SP 800-171 & CMMC

    Defines requirements for protecting controlled and unclassified information for the defense contractors.

  • ITAR & Export-Controlled Quality Processes

    Framework that defines strict regulations to protect information related to defense articles, technical data, and related services from foreign persons.

  • ISO 9001:2026

    Provides the framework for establishing quality management processes to deliver products and services meeting customer and regulatory requirements.

PROOF & RESOURCES

Proven Results. Connected Quality

See how Qualityze QMS software for the Aerospace and Defense industry helps strengthen quality, safety, and compliance controls in one connected ecosystem.

Data-Driven, Defensible Decisions

AI-powered insights grounded in your own data help make defensible decisions, faster.

Closed-Loop Quality Execution

One closed-loop system to manage reviews, release, approvals, investigations, and follow-up actions.

Giant Pharmaceutical Manufacturer logo

Giant Pharmaceutical Manufacturer

Life Sciences

Lower operational costs

Challenge

Manual investigations and email-based approvals delayed deviation closure across multiple manufacturing sites.

Result

Connected workflows improved ownership, accelerated reviews, and linked deviations directly with investigations, CAPA, and effectiveness checks.

Download the Case Study
Medical Device Manufacturer logo

Medical Device Manufacturer

ISO 13485 · FDA

Faster audit preparation

Challenge

Scattered documents and quality records made ISO 13485 and FDA inspection preparation time-consuming.

Result

Centralized records, controlled workflows, and traceable audit evidence helped teams maintain continuous inspection readiness.

Download the Case Study
Growing Biotechnology Company logo

Growing Biotechnology Company

Scaling operations

Lower quality process costs

Challenge

Rapid growth increased quality workloads, while manual processes struggled to scale across teams and programs.

Result

Configurable workflows standardized execution, improved visibility, and supported expansion without adding equivalent administrative overhead.

Download the Case Study

CUSTOMER SUCCESS STORIES

Aerospace & Defense Leaders Trust Qualityze

From clinical-stage biotech to global pharma and medical device manufacturers, quality teams use Qualityze to cut review cycles, close findings faster, and stay continuously inspection-ready.

FROM THE BLOG

Insights on
Modern Quality

Explore practical perspectives on connected quality, compliance, risk, and continuous improvement.

See Qualityze in Action

See how Qualityze connects operational processes and quality data to support better decisions and measurable improvement.

Qualityze
info@qualityze.com+1-877-207-8616

USA Corporate Headquarters

Qualityze Inc.3903 Northdale Blvd Suite: 100ETampa, FL 33624, USA

UK Regional Office

Qualityze Inc.450 Bath Rd, Longford, Heathrow,West Drayton UB7 0EB, United Kingdom

India Regional Office

Qualityze Solutions Pvt Ltd.No. 27, 1st floor, 80 Feet Ring Rd, 2nd Stage,KHB Colony, Basaveshwar Nagar, Bengaluru,Karnataka 560079, INDIAPhone: +91 96117 58187

2015 – 2026 Qualityze Inc