0 Introduction
1 Scope
2 Normative references
3 Definitions
3.1 Product
3.2 Tender
3.3 Contract
4 Quality system requirements
4.1 Management responsibility
4.1.1 Quality policy
4.1.2 Organization
4.1.2.1 Responsibility and authority
4.1.2.2 Resources
4.1.2.3 Management review
4.2 Quality system
4.2.1 General
4.2.2 Quality system procedures
4.2.3 Quality planning
4.2.4 Risk control
4.2.5 Configuration management
4.3 Contract review
4.3.1 General
4.3.2 Review
4.3.3 Amendment to a contract
4.3.4 Records
4.4 Design
4.4.1 General
4.4.2 Design and development planning
4.4.2.1 Work breakdown structure (WBS)
4.4.2.2 Design and development management planning
4.4.2.3 Reliability, availability, maintainability, safety
4.4.3 Organizational and technical interfaces
4.4.4 Design input
4.4.5 Design output
4.4.6 Design review
4.4.7 Design verification
4.4.8 Design validation
4.4.8.1 Testing
4.4.8.2 Justification of definition
4.4.9 Design changes
4.4.9.1 Configuration control
4.4.9.2 Design change approval
4.5 Document and data control
4.5.1 General
4.5.2 Document and data approval and issue
4.5.3 Document and data changes
4.6 Purchasing
4.6.1 General
4.6.2 Evaluation of subcontractors
4.6.3 Purchasing data
4.6.4 Verification of purchased product
4.6.4.1 Supplier verification at subcontractor's premises
4.6.4.2 Customer verification of subcontracted product
4.7 Control of customer-supplied product
4.8 Product identification and traceability
4.9 Process control
4.9.1 General
4.9.1.1 Production documentation
4.9.1.2 Production control
4.9.1.3 Control of production process changes
4.9.1.4 Control of production equipment, tools and N.C.
machine programs
4.9.1.5 Utilities, supplies and workplace environment
4.9.2 Special processes
4.10 Inspection and testing
4.10.1 General
4.10.1.1 Inspection documentation
4.10.1.2 Delegation
4.10.2 Receiving inspection and testing
4.10.3 In-process inspection and testing
4.10.4 Final inspection and testing
4.10.5 Inspection and test records
4.10.6 First article inspection
4.11 Control of inspection, measuring and test
equipment
4.11.1 General
4.11.2 Control procedure
4.12 Inspection and test status
4.12.1 Authorized signatories
4.12.2 Inspection stamps
4.13 Control of nonconforming product
4.13.1 General
4.13.2 Review and disposition of nonconforming product
4.14 Corrective and preventive action
4.14.1 General
4.14.2 Corrective action
4.14.3 Preventive action
4.15 Handling, storage, packaging, preservation and
delivery
4.15.1 General
4.15.2 Handling
4.15.3 Storage
4.15.4 Packaging
4.15.5 Preservation
4.15.6 Delivery
4.16 Control of quality records
4.17 Internal quality audits
4.18 Training
4.19 Servicing
4.20 Statistical techniques
4.20.1 Identification of need
4.20.2 Procedures
Annex A - Bibliography