FDA and EU Process Validation and Equipment Qualification 2019

  • 25-26 Apr 2019
  • DoubleTree by Hilton Hotel Newark Airport, NJ, United States

Description

Topics
  • General Aspects of Qualification
  • Regulatory Requirements and Expectations for Equipment Qualification
  • Performance Qualification and Process Validation
Who should Attend
  • Regulatory Affairs Departments
  • Quality Departments
  • Engineering Departments
  • Compliance Departments
  • Production Departments
  • Manufacturing Departments
  • Validation Teams
  • Operations Departments
  • Process Owners
  • Design Engineers
  • Internal Auditors

Past Events

Important

Please, check "FDA and EU Process Validation and Equipment Qualification" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Operations, Quality assurance
Government & Global Issues: Law & Regulations
Science: Engineering

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