Application of CAPA to the Device Sterilization Process

Application of CAPA to the Device Sterilization Process is a conference that covers topics such as:

  • Basic terms and definitions
  • Introduction to Industrial Sterilization
  • Documenting the EO Validation
  • EO sterilization and Validation processes
  • Typical deficiencies in the EO Process and Validation
  • Maintaining EO Validation
  • Radiation Sterilization and Validation processes
  • Critical and noncritical deficiencies in the EO Process
  • Process validation
  • Determining sterilization dose
  • Documenting the Radiation Validation
  • Maintaining validated sterilization dose
  • Critical and non critical deficiencies in the Radiation Process
  • Typical deficiencies in the Radiation Process and Validation
  • Introduction to CAPA
  • When you should initiate CAPA with your contract sterilizer
  • Why CAPA
  • Applicable regulations and standards
  • Determining Root Cause
  • Defining when to move deficiency to CAPA
  • CAPA tools
  • Determining Actions to Prevent Recurrence

Application of CAPA to the Device Sterilization Process brings together CAPA team members, QA personnel, Quality Engineers, SA personnel and Operations Managers.

Future Events

Application of CAPA to the Device Sterilization Process 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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