Analytical Instrument Qualification and System Validation is a seminar covers topics such as:
- Logic and principles of instrument qualification and system validation from validation planning to reporting
- Regulatory background and requirements for laboratory instrument qualification and system validation
- Execute test protocols, including setting specifications and acceptance criteria
- Company’s qualification and validation strategies
- Developing inspection ready qualification and validation deliverables
- How to review and approve qualification and validation protocols
- How to avoid and/or respond to FDA inspectional observations and warning letters
Analytical Instrument Qualification and System Validation brings together personnel in pharmaceutical development and quality control laboratories and contract testing laboratories, including:
- QA managers and personnel
- IT/IS managers and system administrators
- Analysts
- Laboratory managers and supervisors
- Software developers
- Validation specialists
- Training departments
- Regulatory affairs
- Consultants
- Documentation departments