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GMP MANUAL Volume 2 Validation Procedures
Excerpt from the GMP MANUAL
Auflage: 1st edition 2010
ca. 500 Seiten
Format: DIN A4
ISBN: 978-3-934971-78-3
ca. 500 Seiten
Format: DIN A4
ISBN: 978-3-934971-78-3
€ 175,00
netto
€ 187,25
inkl. 7% MwSt.
x
The second publication in the new GMP MANUAL series contains all important GMP MANUAL chapters about validation procedures:
Qualification
- Official requirements
- Preparation of the qualification
- Qualification documentation
- Design qualification (DQ)
- Installation qualification (IQ)
- Operational qualification(OQ)
- Performance qualification (PQ)
- Special cases of qualification
Process Validation
- Official requirements
- Validation – a key element of quality assurance
- Process validation approaches
- Revalidation
- Planning of process validation projects
- Validation master plan
- Risk analysis
- Validation protocol and report
- Quality by Design
- Process Analytical Technology (PAT)
Cleaning Validation
- Official requirements
- How to validate cleaning procedures
- Cleaning validation master plan
- Establishing the scope of validation
- Acceptance criteria and limit calculation
- Sampling procedures
- Analytical procedures
- Documentation
- Maintenance of the validated status
- Cleaning validation documentation (example)
- References
Computer Validation
- Introduction and basic terminology
- Regulatory aspects
- Life cycle of software and systems
- Risk analysis and system classification
- Validation of computerised systems
- Operation of computerised systems
- External service providers
- References
Full table of contents
Qualification
- Official requirements
- Preparation of the qualification
- Qualification documentation
- Design qualification (DQ)
- Installation qualification (IQ)
- Operational qualification(OQ)
- Performance qualification (PQ)
- Special cases of qualification
Process Validation
- Official requirements
- Validation – a key element of quality assurance
- Process validation approaches
- Revalidation
- Planning of process validation projects
- Validation master plan
- Risk analysis
- Validation protocol and report
- Quality by Design
- Process Analytical Technology (PAT)
Cleaning Validation
- Official requirements
- How to validate cleaning procedures
- Cleaning validation master plan
- Establishing the scope of validation
- Acceptance criteria and limit calculation
- Sampling procedures
- Analytical procedures
- Documentation
- Maintenance of the validated status
- Cleaning validation documentation (example)
- References
Computer Validation
- Introduction and basic terminology
- Regulatory aspects
- Life cycle of software and systems
- Risk analysis and system classification
- Validation of computerised systems
- Operation of computerised systems
- External service providers
- References
Full table of contents
