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El. knyga: Sterile Processing of Pharmaceutical Products: Engineering Practice, Validation, and Compliance in Regulated Environments

  • Formatas: EPUB+DRM
  • Išleidimo metai: 31-Dec-2021
  • Leidėjas: John Wiley & Sons Inc
  • Kalba: eng
  • ISBN-13: 9781119802341
Kitos knygos pagal šią temą:
  • Formatas: EPUB+DRM
  • Išleidimo metai: 31-Dec-2021
  • Leidėjas: John Wiley & Sons Inc
  • Kalba: eng
  • ISBN-13: 9781119802341
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Describes the methodologies and best practices of the sterile manufacture of drug products

Thoroughly trained personnel and carefully designed, operated, and maintained facilities and equipment are vital for the sterile manufacture of medicinal products using aseptic processing. Professionals in pharmaceutical and biopharmaceutical manufacturing facilities must have a clear understanding of current good manufacturing practice (cGMP) and preapproval inspection (PAI) requirements.

Sterile Processing of Pharmaceutical Products: Engineering Practice, Validation, and Compliance in Regulated Environments provides up-to-date coverage of aseptic processing techniques and sterilization methods. Written by a recognized expert with more than 20 years of industry experience in aseptic manufacturing, this practical resource illustrates a comprehensive approach to sterile manufacturing engineering that can achieve drug manufacturing objectives and goals. Topics include sanitary piping and equipment, cleaning and manufacturing process validation, computerized automated systems, personal protective equipment (PPE), clean-in-place (CIP) systems, barriers and isolators, and guidelines for statistical procedure. Offering authoritative guidance on the key aspects of sterile manufacturing engineering, this volume:

  • Covers fundamentals of aseptic techniques, quality by design, risk assessment and management, and operational requirements
  • Addresses various regulations and guidelines instituted by the FDA, ISPE, EMA, MHRA, and ICH
  • Provides techniques for systematic process optimization and good manufacturing practice
  • Emphasizes the importance of attention to detail in process development and validation
  • Features real-world examples highlighting different aspects of drug manufacturing

Sterile Processing of Pharmaceutical Products: Engineering Practice, Validation, and Compliance in Regulated Environments is an indispensable reference and guide for all chemists, chemical engineers, pharmaceutical professionals and engineers, and other professionals working in pharmaceutical sciences and manufacturing.

Preface xiii
Acknowledgments xvii
1 Introduction 1(3)
2 Sterilization 4(11)
Steam Sterilization
5(1)
Flash Sterilization
5(1)
Low-Temperature Sterilization Technologies
6(1)
Ethylene Oxide Gas Sterilization
6(1)
Hydrogen Peroxide Gas Plasma
7(1)
Disinfection and Surface Sterilization Using Peracetic Acid
7(1)
Ionizing Radiation
8(1)
Dry-Heat Sterilizers
8(1)
Filtration
9(1)
Microwave
9(1)
Vaporized Hydrogen Peroxide (VHP*)
9(1)
Ozone
9(1)
Formaldehyde Steam
10(1)
Gaseous Chlorine Dioxide
10(1)
Vaporized Peracetic Acid
10(1)
Infrared Radiation
10(1)
Sterilization Cycle Verification
11(1)
Monitoring
11(4)
3 Sterile Manufacturing Facilities 15(2)
4 Sanitary Process Piping and Equipment 17(32)
QA Procedures
18(1)
Standard Operating Procedures - cGMP Installations
19(1)
Heat Exchangers
19(1)
Sanitary Pumps
20(1)
Sanitary Tanks
20(1)
Instruments
21(1)
Pressure Transmitter (Various Sources)
21(1)
Temperature Transmitter (Various Sources)
21(4)
Standard Operating Procedures - cGMP Installations
25(5)
Surface Finish
30(2)
Welding
32(7)
Applicability
33(6)
Process/Procedure
39(2)
Records (General)
41(3)
Records
44(3)
Automatic Orbital Welding
47(2)
Weld Acceptance Criteria for Automatic Orbital Weld Qualifications
47(2)
5 Passivation 49(14)
In-house Passivation Using Vats
51(2)
Spot Passivation
53(1)
Astro Pak UltraPass Gel Passivation
53(1)
Alternative Process
54(3)
Control of Passivated Items
57(1)
Preparing, Testing, and Adjusting Cleaning and Passivation Chemicals (Passivation in Vats)
58(5)
6 Chilled Water System 63(21)
Process Description
65(10)
Commissioning of HVAC
75(3)
Installation Verification - X Ton Chiller System
78(3)
System Startup - X Ton Chiller
81(1)
Functional Testing - X Ton Chiller
82(2)
7 Clean-In-Place (CIP) Systems 84(11)
Life Cycle Requirements
86(1)
Product and Process User Requirements
86(1)
Process Quality Requirements
86(1)
Process Parameter Requirements
87(4)
Installation User Requirements 87 Operational Requirements
91(4)
8 Computerized Automated Systems 95(75)
Functional Requirement Specification
95(1)
Process Automation System
95(1)
EMS User Requirement Specification
96(2)
Automation Overview
96(1)
Software
97(1)
Hardware
97(1)
SCADA
97(1)
Control Panels
97(1)
Main Control Panel
97(1)
Remote I/O Panels
98(1)
Power Distribution Panels
98(1)
Instrumentation Panels
98(1)
System Functions
98(1)
System Overview
98(1)
Control Modules
99(1)
Interfaces
99(2)
User Interface (SCADA)
99(1)
PAS System Overview
99(1)
Graphical Screen Navigation
99(1)
Client EMS Area Graphical Screens
99(2)
Graphical Control Screens
99(2)
Interfaces to Equipment
101(1)
Interfaces to Other Systems
101(1)
Ethernet Network
101(1)
Nonfunctional Attributes
101(1)
Power Failure Recovery
101(1)
PLC Only Failure
101(1)
HMI Only Failure
101(1)
Network Only Failure
101(1)
Maintainability
102(1)
Backup and Recovery
102(1)
Functional Requirement Specification
102(1)
GLC Environmental Monitoring System
102(1)
Automation Overview
103(2)
System Components
104(1)
Software
104(1)
Hardware
104(1)
Control Panels
104(1)
Gateways
105(1)
System Functions
105(1)
System Overview
105(1)
Control Modules
105(1)
Interfaces
105(1)
User Interface (SCADA)
105(1)
GLC EMS Area Graphical Screen
105(1)
Global Logistics Center (GLC) Environmental Monitoring System
105(1)
Interfaces to Equipment
105(1)
Interfaces to Other Systems
106(1)
Ethernet Network
106(1)
Wireless Connections
106(1)
Nonfunctional Attributes
106(1)
Power Failure Recovery
106(1)
PLC Only Failure
106(1)
HMI Only Failure
106(1)
Network Only Failure
106(1)
Maintainability
107(1)
Backup and Recovery
107(1)
Software Module Design Specification
107(1)
Functional Requirement Specification
108(1)
Process Automation System
108(1)
Automation Overview
109(2)
System Components
109(2)
Software
109(1)
Hardware
110(1)
Control Panels
110(1)
System Functions
111(1)
System Overview
111(1)
Control Modules
111(1)
Interfaces
111(3)
User Interface (SCADA)
111(1)
PAS System Overview Screen
112(1)
Graphical Screen Navigation
112(1)
Graphical Control Screens
112(1)
Interfaces to Equipment
113(1)
Interfaces to Other Systems
113(1)
Ethernet Network
113(1)
Nonfunctional Attributes
114(1)
Power Failure Recovery
114(1)
PLC Only Failure
114(1)
HMI Only Failure
114(1)
Network Only Failure
114(1)
Maintainability
114(1)
Backup and Recovery
114(1)
Software Design Specification
115(1)
Prosoft Configuration
115(1)
Enabling and Disabling of the Gateway Default Server Interface
115(1)
Temperature Sensor Settings
116(1)
Humidity Sensor Settings
116(1)
Software Design Specification
116(2)
Continuous Logic
116(2)
Module Classes and Control Modules
116(1)
Virtual Differential Pressure Alarm Disable
116(1)
Room Condition Indication
117(1)
Navigation Links
117(1)
Alarm Daily Report
118(56)
WFI Still Equipment Module Class
118(8)
WFI Silo Equipment Module Class
126(17)
EM_SILO
126(17)
WFI Primary Loop Equipment Module Class
143(12)
EM_PRIM_LOOP
143(12)
WFI Supply Header Equipment Module Class
155(1)
EM_HEADER
155(7)
Electrical - Controls Equipment Specifications
162(3)
Documentation
165(1)
Drives/Motors
165(5)
9 Personal Protective Equipment (PPE) and Process Flow 170(2)
10 Sterile Aseptic Processing 172(2)
11 Integrated Facility Design 174(6)
Case Study
178(2)
Issue
178(1)
Root Cause
178(1)
Corrective Action
179(1)
Preventive Actions
179(1)
12 Barriers and Isolators 180(3)
Isolator Design Considerations
181(2)
13 Guidelines for Statistical Procedure 183(11)
Process Capability Analysis
184(2)
Long-term Studies
186(1)
Acceptance Sampling
187(3)
Attribute and Variable Sampling Plans
187(1)
Variable Sampling Plans - ANSI Z1.9
188(1)
Normality
188(2)
Transformation of Non-normal Data (Normalization)
190(1)
Protocol Sampling
190(1)
Failure Mode and Effect Analysis (FMEA)
191(3)
Calculating or Recalculating Control Limits
193(1)
14 Calibration 194(11)
Contingency Plan/Disaster Recovery
204(1)
15 Cleaning Validation 205(13)
New Products and Product Changes
208(1)
Cleaning Processes and Changes
208(2)
Risk Assessment/Matrix Approach
209(1)
Matrix Development
209(1)
Cleaning Processes (Manual and Automated)
210(1)
CPP/CQA
210(1)
Cleaning Validation Life Cycle - Cleaning Method Development
211(1)
Strategy for Process Controls
211(1)
Worst-Case Identification - Product/Component
211(5)
Equipment
212(1)
Validation Tests/Inspections - Visual Inspection
212(1)
Chemical Testing
212(1)
Microbiological Testing
213(1)
Endotoxin Testing
213(1)
Sampling Methods
213(1)
Direct Swab Sampling
214(1)
Rinse Sampling
214(1)
Coupon Testing
214(1)
Sampling Sites
214(1)
Acceptance Criteria
214(1)
Residual Levels
214(1)
Endotoxin Levels
215(1)
Microbiological Levels
215(1)
Cleaning Agents/Sanitizer Validation Studies
215(1)
Hold Time Development
216(1)
Dirty Hold Time
216(1)
Clean Hold Time
217(1)
Additional Hold Times/Cleaning Frequencies
217(1)
Continuous Process Verification
217(1)
Failure Investigations
217(1)
16 Validation of Filling Equipment 218(6)
Technical References
223(1)
17 Manufacturing Process Validation 224(8)
Stage 2 - Process Qualification
229(3)
Appendix A Installation Test Plans 232(3)
Appendix B Operational Tests Plans 235(3)
Appendix C WFI Turbulence Flow Requirements 238(1)
Appendix D Water For Injection (WFI) - Design Requirements 239(13)
Process Description
240(1)
Specifications
241(11)
Life Cycle Requirements
241(1)
Product and Process User Requirements
241(2)
Product Description
241(2)
Operating Ranges
243(1)
Material of Construction
244(1)
Metallics
244(1)
Plastics
244(1)
Elastomers
244(1)
Glass
244(1)
Welding Requirements
245(1)
Construction Requirements
246(1)
Lubrication Requirements
247(1)
Electrical Requirements
247(1)
Safety Requirements
247(1)
Operational Requirements
248(2)
Process Constraints and Limitations
248(1)
Process Control System
248(1)
Operator Interface
249(1)
Power Loss and Recovery
250(1)
Cleaning and Sanitizing
250(1)
Maintenance Requirements
250(1)
Training and Documentation Requirements
250(2)
Appendix E Solution Transfer System (STS) - Design Requirements 252(7)
System Description
253(2)
Bulk Powder Handling System
255(4)
Glossary 259(2)
Nomenclature 261(2)
References 263(4)
Further Reading 267(68)
Index 335
Sam A. Hout, PhD, MBA, is a Chartered Chemical Engineer, certified in business management by the American Production and Inventory Control Society (APICS), and a member of the International Society of Pharmaceutical Engineers (ISPE). Dr. Hout held the position of Senior Director of Engineering, project management, and technology process transfers at Siegfried Pharmaceuticals. Previously, he was Senior Manager of Engineering at TEVA Pharmaceuticals and Director of Operations at the HPLC company Phenomenex.