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Validation of Equipment


  • Validation of Equipment

    • Overview

    Equipment Validation
    Based on the concept of risk management, validation shall be performed for systems or equipment which can impact the quality, process or control of the product. Austar has experienced engineers for various kinds of pharmaceutical production equipment and their validation. We can provide GMP compliant commissioning and qualification services for any production equipment of our customers.
        Equipment mainly includes:

      - Process equipment for sterile preparations
      - Process equipment for oral solid dosages
      - Process equipment for APIs
      - Process equipment for sterile APIs
      - Process equipment for biological products
      - Packaging equipment
      - Cleaning and sterilization equipment
      - Auxiliary equipment

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