Analytical Instrument Qualification and System Validation

Description

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

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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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