Analytical Instrument Qualification and System Validation

  • 06-07 Feb 2020
  • DoubleTree by Hilton Hotel San Francisco Airport, Burlingame, CA, United States

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

Past Events

Important

Please, check "Analytical Instrument Qualification and System Validation" official website for possible changes, before making any traveling arrangements

Event Categories

Science: Laboratories, Life Sciences & Biology

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