- ACTIVE PHARMACEUTICAL INGREDIENTS
- BIOTECHNOLOGY
- CLEANING VALIDATION
- COMMISSIONING AND QUALIFICATION
- Commissioning and Qualification of Pharma Water & Steam Systems 2nd Edition
- Product Quality Lifecycle Implementation (PQLI®) from Concept to Continual Improvement Part 1: Product Realization using QbD, Concepts and Principles
- Product Quality Lifecycle Implementation (PQLI® ) from Concept to Continual Improvement Part 2: Product Realization using QbD, Illustrative Example
- Baseline Guide Volume 5: Commissioning & Qualification 2nd Edition
- CONTAINMENT
- Assessing the Particulate Containment Performance of Pharmaceutical Equipment (Second Edition)
- Cleaning Validation Lifecycle - Applications, Methods, & Controls
- Containment for Potent Compounds
- ISPE D/A/CH Affiliate: Containment Manual (English Translation)
- Maintenance
- Risk-Based Manufacture of Pharmaceutical Products (Risk-MaPP)
- CRITICAL UTILITIES
- DISPOSABLES
- ENGINEERING STANDARDS BENCHMARKING
- GAMP®
- GAMP® 5: A Risk-Based Approach to Compliant GxP Computerized Systems
- A Risk-Based Approach to Calibration Management (Second Edition)
- A Risk-Based Approach to GxP Compliant Laboratory Computerized Systems (Second Edition)
- A Risk-Based Approach to GxP Process Control Systems (Second Edition)
- A Risk-Based Approach to Operation of GxP Computerized Systems
- A Risk-Based Approach to Regulated Mobile Applications
- A Risk-Based Approach to Testing of GxP Systems (Second Edition)
- Electronic Data Archiving
- Global Information Systems Control and Compliance (Second Edition)
- IT Infrastructure Control and Compliance (Second Edition)
- Manufacturing Execution Systems – A Strategic and Program Management Approach
- RDI Good Practice Guide: Data Integrity by Design
- Records and Data Integrity
- Validation and Compliance of Computerized GCP Systems & Data [Good eClinical Practice]
- GOOD CONTROL LABORATORY PRACTICES
- HEATING, VENTILATION, AND AIR CONDITIONING
- INVESTIGATIONAL PRODUCTS
- Cleaning Validation Lifecycle - Applications, Methods, & Controls
- Clinical Supply Systems
- Comparator Management
- Development of Investigational Therapeutic Biological Products
- Harmonizing the Definition and Use of Non-Investigational Medicinal Products (NIMPs)
- Interactive Response Technology
- Maintenance
- OPERATIONS MANAGEMENT
- ORAL SOLID DOSAGE
- PACKAGING
- PROCESS ANALYTICAL TECHNOLOGY (PAT)
- PROCESS/PRODUCT DEVELOPMENT
- Approaches to Commissioning and Qualification of Pharmaceutical Water and Steam Systems (Second Edition)
- Cleaning Validation Lifecycle - Applications, Methods, & Controls
- Good Practice Guide: Technology Transfer 3rd Edition
- Maintenance
- Product Quality Lifecycle Implementation (PQLI®) from Concept to Continual Improvement Part 1: Product Realization using QbD, Concepts and Principles
- Product Quality Lifecycle Implementation (PQLI®) from Concept to Continual Improvement Part 2: Product Realization using QbD, Illustrative Example
- Product Quality Lifecycle Implementation (PQLI®) from Concept to Continual Improvement Part 3: Change Management System as a Key Element of a Pharmaceutical Quality System
- Product Quality Lifecycle Implementation (PQLI®) from Concept to Continual Improvement Part 4: Process Performance and Product Quality Monitoring System (PP&PQMS)
- PROJECT MANAGEMENT
- QUALITY MANAGEMENT
- STERILE PRODUCTS PROCESSING (SPP)
- SUSTAINABLE FACILITIES
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