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      PK-VF In-line Flowpacks and Pouches Tester

      Pharmaceuticals

      Non-Invasive, Non-Destructive, 100% in-line Integrity Inspection at high production speed

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      IV Bags

      Pouches

      Flowpacks

      Tech specifications
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      Highlights

      • Autotest in real time
      • Easy to validate
      • CFR 21 part 11 compliance and 4.0 full integration
      • Quick format changeover
      • High installation flexibility
      Contact Us
      PK-VF | In-line Flowpacks and Pouches Tester Contact Us
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      Technical Features

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      • Container Application: IV Bags, Flowpacks & Pouches
      • Products: Semi-solid, Powder, Liquid
      • Container Dimensions: 40 x 40 x 10 mm (min); 150 x 150 x 50 mm (max)
      • Speed: Up to 180 Cpm
      • Technology: CCIT
      • Inspection features: Non-Invasive, Non-Destructive CCIT based on Vacuum Decay Method
      • Inspection Capabilities: Microleaks detection
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      Additional Benefits

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      • Full batch control testing: fast, reliable and repeatable
      • Testing of all nominal production line speed
      • MES (Manufacturing Execution System connection) allows remote machine data exchange & download
      • Statistical Process Control reduces deviations for a better yield control
      • Real time display of testing cycle diagrams, statistical raw data
      • Easy, quick and safe remote access
      • AHE (Automatic Head Exclusion)
      • Easy cleaning
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      Technology

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      • Container Closure Integrity Testing is a non-destructive measurement technology based on Vacuum Decay Method.
        Measurement system comprises applying a pressure differential into an airtight testing group enclosing the container.
        The test objective is to detect container leakages by measuring the reached vacuum level as well as the vacuum change over test time.
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      Quality Assurance

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      • Equipment test method refers to:
        • Approved industry standard “ASTM F2338-09”: “Standard Test Method for Non-Destructive Detection of Leaks in Packages”
        • United States Pharmacopoeia – USP General Chapter «1207» “Packaging Integrity Evaluation”
        • EU Guidelines to GMP Medicinal Products for Human and Veterinary Use – Annex 1 “Manufacture of Sterile Medicinal Products”
        • PDA Technical Report No. 27 “Pharmaceutical Package Integrity”
        • FDA 21 CFR part 11 as well as EMA Annex 11

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