Connecticut Spring and Stamping

Activities: Manufacturing Medical Devices

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  1. What is ISO 8 cleanroom classification? Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
  2. Identifying and preventing contaminant leakage from your cleanroom A common solution to machinery contamination in a cleanroom is to build a cleanroom within a cleanroom using partitions or curtains, to isolate the machine. Chris Lindlar from...
  3. Integrity testing of HEPA filters: A practical approach Filtering the air in aseptic process areas is critical to maintaining the cleanliness of the production environment. Jesus Casas provides tips to ensure HEPA filters are fit...
  4. Industry 4.0: What is the advantage of real-time digital signage? Olivia Fernandez from Digital Therapeutics (DTx) disusses how digital signage can serve in cleanrooms as a versatile and powerful tool that allows those in charge to ensure...
  5. Legionella testing: Modern alternatives to the ‘gold standard’ test The development of significantly faster, more sensitive testing protocols provide more options for detection Legionella than the complex plate culture test, but these also have...

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Manufacturing

Springing into action

Not all component production for medical devices currently requires a cleanroom or ISO 13485 certification but Steve Dicke, Connecticut Spring and Stamping, believes the writing is on the wall
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