- Annual Product Quality Review (APQR)
- Annual Product Review (APR)
- Aseptic Processing
- Audit
- Batch Record
- Batch Release
- Batch Release Certificate
- Batch Release Documentation
- Batch Release Testing
- Calibration
- Change Control
- Change Management
- Cleaning Validation
- Clean-in-Place (CIP)
- Cleanroom
- Compliance
- Corrective Action Plan
- Corrective and Preventive Actions (CAPA)
- Critical Control Point (CCP)
- Critical Process Parameter (CPP)
- Critical Quality Attribute (CQA)
- Data Integrity
- Design Control
- Deviation
- Documentation
- Environmental Monitoring
- Environmental Monitoring Program
- Equipment Maintenance
- Equipment Qualification
- Failure Investigation
- Good Documentation Practices (GDP)
- Good Manufacturing Practices (GMP)
- In-Process Controls
- Investigation
- Master Batch Record
- Material Management
- Material Qualification
- Ongoing Process Verification (OPV)
- Out of Specification (OOS)
- Packaging and Labeling Control
- Preventive Maintenance
- Process Capability
- Process Capability Index (Cpk)
- Process Mapping
- Process Monitoring
- Process Optimisation
- Process Performance Qualification (PPQ)
- Process Validation
- Product Complaints
- Qualification
- Quality Agreement
- Quality Assurance
- Quality Control Laboratory
- Quality Control Release Testing
- Quality Control Sampling
- Quality Management Review
- Quality Management System (QMS)
- Quality Metrics
- Quality Risk Assessment
- Quality Risk Management
- Qualty Control (QC)
- Raw Material Testing
- Record Retention
- Regulatory Compliance
- Requalification
- Retrospective Validation
- Risk Assesment
- Risk Assessment Matrix
- Risk-Based Approach
- Root Cause Analysis (RCA)
- Stability Program
- Stability Testing
- Standardisation
- Standard Operating Procedure (SOP)
- Sterilisation Validation
- Supplier Audit
- Supplier Qualification
- Training
- Trend Analysis
- Validation
- Vendor Qualification
Glossary
- Mozeka Limited
- Glossary
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