Analytical Instrument Qualification and Validation – Understanding Use of Excel and FDA Audit Preparation 2019

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.

Topics

• 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

Who should Attend

• 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