Equipment Qualification and Process Validation

Equipment Qualification and Process Validation is a webinar dedicated to FDA requirements for qualification and validation.

Equipment Qualification and Process Validation covers topics such as:

  • Equipment Qualification
  • General FDA GMP information requalification and validation
  • Manufacturing and Cleaning Process Validation
  • Computer System Qualification and Part 11

Equipment Qualification and Process Validation is intended for:

  • Personnel responsible for computer system qualification
  • Personnel responsible for equipment qualification
  • Personnel responsible for cleaning validation
  • Personnel responsible for manufacturing process validation
  • Quality Professionals
  • Regulatory Affairs, Regulatory Compliance

Future Events

Equipment Qualification and Process Validation 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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