Validation Engineer - Process Validation & System Calibration

An Introduction to Validation & Methods of Sterilization

Contributes 30 minutes to your CPD

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Course Details:

This course provides a concise historic overview on the development of validation, the stages of validation (DQ/IQ/OQ/PQ), and an overview of sterilization types such as Steam (Moist Heat), Dry Heat, ETO and Formaldehyde.

Please Note: This course is meant as a refresher only for qualified validation engineers and is not an alternative to industry recognised CP(D) qualifications.

Aims:

To provide an overview of validation, the various stages of validation, and types of sterilization and loads able to be processed.

Objectives:

The learner will be able to:

  • Describe the various stages of validation (DQ/IQ/OQ/PQ).
  • Understand the definition of Sterile and F0
  • Understand the differences between sterilization methods, and the loads able to be processed. 

Learning Outcomes:

The learner understands:

  • Validation terminology.
  • The definition of Sterile and F0
  • Different methods of sterilization and loads.