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· 분류 : 외국도서 > 과학/수학/생태 > 과학 > 화학 > 분석화학
· ISBN : 9781119529231
· 쪽수 : 320쪽
· 출판일 : 2020-06-03
목차
Preface
1. Chapter 1: Introduction to the Quality Systems Based Approach to CGMP Compliance
1.1. Overview of Quality Systems and the Laboratory Control System
1.2. Regulations and Regulatory Bodies
1.3. Regulatory Guidance
1.4. Application of This Text
1.5. Overlap and Redundancy
1.6. Tools and Templates
1.7. References
2. Chapter 2: Components of the Laboratory Managerial and Administrative Systems Sub Element (MS)
2.1. Description of the Laboratory Managerial and Administrative System Sub Element
2.2. Contents of the Sub Element
2.3. Tools and Templates
2.4. References
3. Chapter 3: Components of the Laboratory Documentation Practices and Standard Operating Procedures Sub Element (OP)
3.1. Description of the Laboratory Documentation Practices and Standard Operating Procedures Sub Element
3.2. Contents of the Sub Element
3.3. Tools and Templates
4. Chapter 4: Components of the Laboratory Equipment Sub Element (Le)
4.1. Description of the Laboratory Equipment Sub Element
4.2. Contents of the Sub Element
4.3. Tools and Templates
4.4. References
5. Chapter 5: Components of the Laboratory Facilities Sub Element (LF)
5.1. Description of the Laboratory Facilities Sub Element
5.2. Contents of the Sub Element
5.3. Tools and Templates
5.4. References
6. Chapter 6: Components of the Method Validation and Method Transfer Sub Element (MV)
6.1. Description of the Method Validation and Method Transfer Sub Element
6.2. Contents of the Sub Element
6.3. Tools and Templates
6.4. References
6.5. Glossary
7. Chapter 7: Components of the Laboratory Computer Systems Sub Element (LC)
7.1. Description of the Laboratory Computer Systems Sub Element
7.2. Contents of the Sub Element
7.3. Tools and Templates
7.4. References
7.5. Glossary
8. Chapter 8: Components of the Laboratory Investigations Sub Element (Li)
8.1. Background and Regulatory History of Out-of-Specification Investigations
8.2. Description of the Laboratory Investigations Sub Element
8.3. Contents of the Sub Element
8.4. Tools and Templates
8.5. References
8.6. Glossary
9. Chapter 9: Components of the Laboratory Data Governance and Data Integrity Sub Element (DI)
9.1. Background
9.2. Precepts Regarding Data Governance and Data Integrity
9.3. Description of the Laboratory Data Governance and Data Integrity Sub Element
9.4. Contents of the Sub Element
9.5. Tools and Templates
9.6. References
9.7. Bibliography
9.8. Glossary
10. Chapter 10: Components of the Stability Program Sub Element (SB)
10.1. Description of the Stability Program Sub Element
10.2. Content of the Sub Element
10.3. Tools and Templates
10.4. References
10.5. Glossary
11. Chapter 11: Components of the General Laboratory Compliance Practices Sub Element (CP)
11.1. Description of the General Laboratory Compliance Practices Sub Element
11.2. Content of the Sub Element
11.3. Tools and Templates
12. Chapter 12: Summary for Establishing and Maintaining a Laboratory Control System
12.1. A Brief Review of the Laboratory Control System and Its Sub Elements
12.2. How Things Can Go Wrong: Examples of Some Regulatory Citations
12.3. Some Final Thoughts on Establishing and Maintaining a Compliant Laboratory Control System
Index














