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

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

Future Events

Analytical Instrument Qualification and Validation – Understanding Use of Excel and FDA Audit Preparation 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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