Analytical Instrument Qualification and Validation Understanding Use of Excel and FDA Audit Preparation 2019 is a conference dedicated to In this two day workshop conference you will learn the different global agencies expectations of analytical equipment.
Analytical Instrument Qualification and Validation Understanding Use of Excel and FDA Audit Preparation 2019 covers topics such as:
- The logic and principles of instrument qualification and system validation from validation planning reporting
- The regulatory background and requirements for laboratory instrument qualification and system validation
- Preparing and executing test protocols
- Company’s qualification and validation strategies
- Validation and Use of Excel in the QC Laboratory
- How to review and approve qualification and validation protocols
- Developing inspection ready qualification and validation deliverables
- Handling raw data and other laboratory records
- How to avoid and/or respond to FDA inspectional observations and warning letters
Analytical Instrument Qualification and Validation Understanding Use of Excel and FDA Audit Preparation 2019 brings together:
- IT managers and staff
- Laboratory managers, supervisors and analysts
- Laboratory suppliers of material, equipment and services
- Consultants
- Quality professionals
- Senior quality managers
- Compliance professionals
- Regulatory professionals
- Validation engineers
- Production supervisors
- Production engineers
- Manufacturing engineers
- Process owners
- Design engineers
- Quality auditors
- Quality engineers
