AS9120B
Aerospace QMS standard for distributors' traceability and counterfeit prevention
ISO 27701
International standard for privacy information management systems
Quick Verdict
AS9120B ensures quality management for aerospace distributors via traceability and counterfeit controls, while ISO 27701 establishes PIMS for privacy accountability. Distributors adopt AS9120B for OEM approval; all PII handlers use ISO 27701 for regulatory trust and certification.
AS9120B
AS9120B:2016 Quality Management Systems for Distributors
Key Features
- Rigorous traceability and chain-of-custody controls for split lots
- Counterfeit and suspected unapproved parts prevention processes
- Risk-based external provider evaluation and flowdown requirements
- Configuration management tailored to distribution operations
- Enhanced product safety and ethical behavior awareness
ISO 27701
ISO/IEC 27701:2025 Privacy Information Management
Key Features
- PIMS framework extending ISO 27001 for privacy
- Separate controls for PII controllers and processors
- Risk-based assessments and DPIAs
- GDPR and regulatory mappings in annexes
- PDCA cycle for continual improvement
Detailed Analysis
A comprehensive look at the specific requirements, scope, and impact of each standard.
AS9120B Details
What It Is
AS9120B:2016 is a certification standard for quality management systems (QMS) tailored to aerospace distributors who procure, store, split, and resell parts without alteration. Built on ISO 9001:2015's 10-clause high-level structure, it adds over 100 IAQG-specific requirements using a risk-based approach to address distribution risks like traceability loss and counterfeits.
Key Components
- Core pillars: context analysis, leadership, planning, support, operations, evaluation, improvement.
- Distributor-focused: traceability, counterfeit prevention, external provider controls, configuration management.
- Over 100 aerospace additions beyond ISO 9001.
- Certification via accredited bodies, OASIS listing for visibility.
Why Organizations Use It
- Commercial necessity for OEM/Tier-1 supply chains.
- Mitigates risks of nonconformities, recalls, legal liabilities.
- Builds customer trust, market access (2,442 global certifications).
- Drives efficiency, reduces defects via standardized processes.
Implementation Overview
- Phased: gap analysis, process design, training, audits (6-12 months).
- Applies to aviation/space/defense distributors globally.
- Involves cross-functional teams, Management Representative, IAQG-grade audits.
ISO 27701 Details
What It Is
ISO/IEC 27701:2025 is the international standard for establishing, implementing, maintaining, and improving a Privacy Information Management System (PIMS). It provides a risk-based framework for managing personally identifiable information (PII) lifecycle, extending ISO/IEC 27001 with privacy-specific requirements for PII controllers and processors.
Key Components
- Clauses 4–10 mirroring ISO management systems, plus Annex A (controller controls) and Annex B (processor controls).
- Core areas: governance, PII inventory, DPIAs, data subject rights, third-party management, cross-border transfers.
- Built on PDCA cycle; includes GDPR mappings (Annex D).
- Certification via accredited bodies with 3-year validity and surveillance audits.
Why Organizations Use It
- Demonstrates accountability for global privacy laws like GDPR.
- Mitigates regulatory fines, breach risks, and supply-chain exclusions.
- Enhances trust, competitive edge in B2B markets, insurance benefits.
Implementation Overview
- Phased PDCA approach: discover/scope, design/plan, implement/operate, validate/improve.
- Applicable to all sizes/industries handling PII; integrates with ISMS.
- Requires PII mapping, policies, training, audits for certification.
Key Differences
| Aspect | AS9120B | ISO 27701 |
|---|---|---|
| Scope | Aerospace distribution QMS, traceability, counterfeit prevention | Privacy Information Management System, PII lifecycle, data protection |
| Industry | Aviation, space, defense distributors globally | All sectors handling PII worldwide |
| Nature | Voluntary IAQG certification standard | Voluntary ISO privacy management certification |
| Testing | IAQG audits, internal audits, management reviews | Certification audits, internal audits, surveillance audits |
| Penalties | Loss of certification, market exclusion | Loss of certification, no direct legal penalties |
Scope
Industry
Nature
Testing
Penalties
Frequently Asked Questions
Common questions about AS9120B and ISO 27701
AS9120B FAQ
ISO 27701 FAQ
You Might also be Interested in These Articles...

Why the SEC Stepped In: The Investor-Driven Push for Cybersecurity Transparency
Discover why the SEC's 2023 cybersecurity rules treat cyber risks as material financial threats. Explore the 'stick and carrot' approach for standardized disclo

5 Ways Modern Compliance Software Makes Evolving Regulations Your Strategic Advantage
Discover 5 ways modern compliance software turns evolving regulations into strategic advantage. Automate monitoring, cut 3x non-compliance costs, stay audit-rea

The Reasons Why NIS2 is Fundamental for Cyber Resilience in Europe
Uncover why NIS2 transcends compliance burdens, delivering real cyber resilience value through enforced measurements and activities. Explore insights via our pa
Run Maturity Assessments with GRADUM
Transform your compliance journey with our AI-powered assessment platform
Assess your organization's maturity across multiple standards and regulations including ISO 27001, DORA, NIS2, NIST, GDPR, and hundreds more. Get actionable insights and track your progress with collaborative, AI-powered evaluations.
Check out these other Gradum.io Standards Comparison Pages
NIST CSF vs CSL (Cyber Security Law of China)
Compare NIST CSF vs CSL: voluntary US framework meets China's mandatory cybersecurity law. Key diffs in governance, data localization & risk mgmt—master global compliance now.
LGPD vs AEO
LGPD vs AEO: Compare Brazil's data privacy law with global trade security standards. Key differences, compliance tips & strategies for multinationals. Master both now!
CCPA vs FDA 21 CFR Part 11
Compare CCPA vs FDA 21 CFR Part 11: Key compliance differences, strategies, pitfalls & frameworks for privacy rights & electronic records. Ensure mastery now.