FDA and EU Process Validation and Equipment Qualification

FDA and EU Process Validation and Equipment Qualification is a seminar that covers topics such as:

  • General Aspects of Qualification
  • Regulatory Requirements and Expectations for Equipment Qualification
  • Performance Qualification and Process Validation

FDA and EU Process Validation and Equipment Qualification brings together:

  • Regulatory Affairs Departments
  • Quality Departments
  • Engineering Departments
  • Compliance Departments
  • Production Departments
  • Manufacturing Departments
  • Validation Teams
  • Operations Departments
  • Process Owners
  • Design Engineers
  • Internal Auditors

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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