Cleanliness Testing

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  • Circuit Board Cleanliness Testing
    Contamination of circuit boards can bring about severe degradation of insulation resistance and dielectric strength. This application bulletin explains how a simple "on line" test for the relative measurement of ionic contamination using a conductivity meter has been developed to determine
  • What Medical Device Manufacturers Need from Surface Cleanliness Testing
    Quality tests during medical device production need to check a lot of boxes for manufacturers. Testing must increase confidence in product reliability in order to be worthwhile to manufacturers. What's more, that confidence needs to be measurable and reportable because companies cannot tolerate
  • Automotive Standards for Technical Cleanliness
    The demand for quality control of components and cleanliness testing have risen steadily in recent years-so much so that clean manufacturing is now one of the main issues in the automotive industry. Both functionality and the lifetime of products are linked directly to the extent of particulate
  • CIP Systems Raise the Bar on Cleanliness
    . But it also has a fairly comprehensive laboratory that includes wind tunnels, atomization analysis and other tools to analyze sprayer performance. Swagelok, Inc. (Solon, Ohio) has performed extensive computer testing of its fittings, using computational fluid dynamics (CFD) to model flow patterns. In one
  • Breaking Down the Technical Cleanliness Workflow Part 4: Contamination Level Calculation
    In the fourth of this six-part blog series, we explore how contamination levels are calculated, including defining cleanliness codes and testing maximum approvals.
  • ISO-4406 Hose Cleaning Test Report (.pdf)
    This ISO-4406 test report shows the cleanliness differences between an un-cleaned hose VS an air blown Hose VS a hose cleaned with the Ultra Clean System
  • Application of Ultrasonic Cleaning
    . A few examples of measuring cleanliness include various levels of particle count, microscopic inspection, and a variety of adhesion tests, including the clear tape test that has the ability to remove additional contamination. These are just a few examples of cleanliness measurement.
  • Containment Technologies Group
    verification and monitoring of airborne particulate cleanliness. Factors required under this section include frequency, environmental test conditions, and particle counting. Frequency indicates that,
  • Does Heat Really Affect Protection? Poster Download
    Heat sources in a Biosafety Cabinet Compromise Experimental and User Protection. Several heat sources were evaluated in two sizes of BSC, using smoke for airflow visualization, particle counting for air cleanliness, and aerosol microbiological testing to show containment.
  • How Clean Is Clean Enough?
    Cleaning assessment and validation of medical devices has received increased scrutiny from the medical device industry and regulatory agencies in the past 10 years. Cambridge Polymer Group provides testing services on cleanliness of medical devices, for both quantification and identification
  • New Model Workstation HEPA Performance Report
    The Invivo2 / Concept / Concept-M Series Workstations have been recently remodelled, and now include a standard HEPA filter. This report details the HEPA filter testing and results for the common body of these workstations to determine air cleanliness using EN ISO 14644-1 as a reference
  • Medical Specimen Transport System Success Story
    An OEM wanted to launch a solution to provide hospitals and laboratories with an automation material handling solution for transporting fragile test tube specimens within a laboratory setting. Our client required absolute cleanliness, rigorous maintenance and zero-risk safety standards for handling
  • Products & Services 2
    contains: a polymer mix/dispense system, coagulant addition system, product feed pump, solids discharge system, water testing instruments to gage water cleanliness, and an effluent return system with a pump to return the liquid to the source. Cartridge Filters Maximize Efficiency for High Protein
  • Key Considerations for Medical Device Design
    solutions. Regulatory: *FDA, UL, IEC (Agency Requirements). *Creepage/Clearance/Isolation. *Patient Connect Requirements. *Patient Contact Requirements. Quality & Reliability: *Cleanliness. *Unique Test Requirements. *Materials & Process Traceability (Six Sigma CPK levels). *Minimized Process Variation
  • Getting the Most from Coriolis Flowmeters in Pharmaceutical Processes
    , measurement accuracy and cost consciousness, the industry provides some specific challenges for flow measurement technology. With the variety of processing steps and the need for cleanliness, purity and rigorous accountability to consumers and regulators, there is a need for a flow technology
  • Containment Technologies Group
    , the authors tested a barrier isolator system at the University of Cincinnati Hospital. The results are presented here. - barrier/isolator technology: cleanrooms: parenteral drugs Providing a facility for the manipulation of parenteral drugs within the pharmacy is a significant concern for health care