Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing

The Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing is a seminar that covers topics such as:

  • Documents required for equipment qualification and process validation and how to manage documents appropriately
  • The global expectations for equipment qualification and validation
  • Write and execute sound protocols for equipment qualification (IQ, OQ, PQ) and process validation
  • How to write and maintain a Validation Master Plan
  • Collect data, conduct tests, and obtain all necessary documents
  • Qualify already existing systems and requalification
  • Performance Validation
  • The different types of validation
  • The principles of auditing the equipment qualification and validation
  • Validating analytical methods and processes
  • How to investigate true root causes of problems and to evaluate and prioritize solutions
  • External qualification and validation from a contract manufacturer, and qualification and validation by a supplier
  • Develop successful implementation plans
  • Problem solving methods to help you asses which is best for your situation
  • Perform risk assessments effectively

The Global Regulations for Equipment Qualification and Validation of Processes in the Pharma Manufacturing brings together:

  • Quality professionals
  • Senior quality managers
  • Compliance professionals
  • Regulatory professionals
  • Validation engineers
  • Production supervisors
  • Production engineers
  • Manufacturing engineers
  • Process owners
  • Design engineers
  • Quality auditors
  • Quality engineers
  • Document control specialists

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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