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- APQP - Advanced Product Quality Planning
- Adverse event
- ANSI - American National Standards Institute
- ASQ - American Society for Quality
- ANSI/AIHA Z10-2005
- Assessment
- AS/NZS 4360
- AS/NZS 4360
- Basel II
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- BS8800
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- ci-continuous-improvement
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- COSO ERM
- CCM - Customer Complaint Management
- CRM - Customer Relationship Management/ IBS America
- Defect
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- Document control
- DHF - Design History File
- DHR - Device History Record
- DMR - Device Master Record
- ECO - Engineering Change Order
- ECR - Engineering Change Request
- EMI - Enterprise Manufacturing Intelligence
- Environmental aspects
- EH&S - Environmental, Health and Safety
- Environmental impacts
- FDA 21 CFR Part 11
- FDA 21 CFR Part 11
- FDA 21 CFR Part 820 / Quality System Regulations
- GMS - Gage Management System
- GR and R - Gage repeatability and reproducibility
- Gandtt chart
- GMP - Good manufacturing practices
- GRC - Governance, Risk Management, and Compliance
- HIPAA
- IGOG - Incoming Goods/Outgoing Goods Control
- Inspection plan
- Inspection Plan Management (IPM)
- ISO 9000
- ISO 13485
- ISO 14000
- ISO/TS 16949
- KPI - Key performance indicator
- Lean manufacturing
- Lean Six Sigma
- MES - Manufacturing Execution System
- MOM - Manufacturing Operations Management
- NCMR - Nonconforming Material Request
- Nonconformity
- OH & S - Occupational Health & Safety
- OCEG - Red Book
- OHSAS 18000
- OEM - Original equipment manufacturer
- Pareto chart
- Preventative action
- PLM - Product Lifecycle Management
- Production Part Approval Process
- Production Quality Management
- Quality Control
- Quality management
- Quality Management system
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- Responsible Care
- Return Material Authorization
- Risk management
- Root cause
- SOX - Sarbanes Oxley Act
- Six Sigma
- Statistical process control
- Total Quality Management
- Validation
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- Zero defects
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