Quality assurance is a critical component of the pharmaceutical industry, as it ensures that products meet the required quality standards and comply with regulatory requirements. Quality assurance includes a range of activities, such as document control, change control, deviation management, CAPA management, vendor qualification, and audit management.
Here is a list of SOPs related to quality assurance:
SOP for Document Control
SOP for Change Control
SOP for Deviation Management
SOP for Corrective and Preventive Action (CAPA) Management
SOP for Vendor Qualification
SOP for Audit Management
SOP for Quality Management Review (QMR)
SOP for Quality Risk Management
SOP for Failure Investigation
SOP for Batch Record Review
SOP for Sample Management
SOP for Complaint Handling
SOP for Recall Management
SOP for Stability Study Management
SOP for Calibration Management
SOP for Preventive Maintenance
SOP for Validation Master Plan
SOP for Equipment Qualification
SOP for Facility Qualification
SOP for Computer System Validation
SOP for Data Integrity Management
SOP for Training Management
SOP for Performance Qualification
SOP for Cleaning Validation
SOP for Process Validation
SOP for Analytical Method Validation
SOP for Statistical Process Control (SPC)
SOP for Quality Control (QC) Sample Preparation
SOP for Environmental Monitoring
SOP for Microbial Identification
SOP for Bioburden Monitoring
SOP for Sterility Assurance
SOP for Water System Validation
SOP for Media Fill
SOP for Aseptic Processing
SOP for Good Manufacturing Practices (GMP) Compliance
SOP for Good Laboratory Practices (GLP) Compliance
SOP for Good Clinical Practices (GCP) Compliance
SOP for Good Distribution Practices (GDP) Compliance
SOP for Good Documentation Practices (GDP) Compliance
SOP for Raw Material Management
SOP for Finished Product Release
SOP for Label Control
SOP for Batch Release
SOP for Stability Testing
SOP for Retention Sample Management
SOP for Disposition of Nonconforming Materials
SOP for Risk Assessment
SOP for Quality Agreement Management
SOP for Batch Manufacturing Record (BMR) Preparation
SOP for Batch Packaging Record (BPR) Preparation
SOP for Data Review and Approval
SOP for Master Formula Record (MFR) Preparation
SOP for Master Packaging Record (MPR) Preparation
SOP for Product Quality Review (PQR) Preparation
SOP for Out of Specification (OOS) Investigation
SOP for Out of Trend (OOT) Investigation
SOP for Change Notification
SOP for Product Development
SOP for Intellectual Property Management
SOP for Compliance Management
SOP for Data Retention
SOP for Archiving
SOP for Records Management
SOP for Information Security Management
SOP for Crisis Management
SOP for Emergency Response
SOP for Business Continuity Planning (BCP)
SOP for Disaster Recovery Planning (DRP)
SOP for Incident Management
SOP for Internal Audit
SOP for External Audit
SOP for Risk Management Plan
SOP for Risk Mitigation
SOP for Risk Communication
SOP for Risk Monitoring and Control
SOP for Quality Metrics Management
SOP for Product Complaint Investigation
SOP for Quality Control of Raw Materials
SOP for Change Implementation
SOP for Change Evaluation
SOP for Change Notification
SOP for Inspection Management
SOP for Sample Analysis
SOP for Laboratory Investigation
SOP for Root Cause Analysis
SOP for Corrective Action Plan (CAP) Development
SOP for Performance Monitoring and Evaluation
SOP for Continuous Improvement Program
SOP for Non-Conformance Management
SOP for Corrective Action Plan (CAP) Execution
SOP for Preventive Action Plan (PAP) Development
SOP for Preventive Action Plan (PAP) Execution
SOP for Management Review
SOP for Supplier Evaluation
SOP for Supplier Auditing
SOP for Supplier Management
SOP for Supplier Quality Agreement Management
SOP for Material Review Board (MRB) Management
SOP for Customer Complaint Investigation.
