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  • A Review of Analytical Methodologies in PM Analysis
    An attempt has been made to review a broad range of methodology currently in use at labs providing services to the precious metals industry. Preference of a particular technique may vary from one lab to another. Very often this choice is based upon the range of equipment available for assay
  • Medical Device Link .
    Bringing an assay from lab bench to marketplace involves a diverse range of skills and experience. Careful planning, milestones, and other production goals are key to this process, and assay development requirements have been documented in a number of books. Beyond these basic concerns, however
  • Medical Device Link .
    , rugged, low-cost, and easy-to-use diagnostic instruments that offer high levels of capability and versatility. Microfluidics fluids flowing in microchannels makes possible the design of analytical devices and assay formats that would not function on a larger scale. Figure 1. Flow schematic of an H-filter
  • Medical Device Link .
    or individual researchers. In the late 1980s, several companies had R&D groups performing rapid-assay work. Many of these original companies have gone on to spawn new businesses. At the time, communication between scientists was rare, and was very much the exception rather than the rule. During
  • Medical Device Link .
    . The cap worked so well that rising customer demand for its use in other Gen-Probe assay kits promised to exceed the company's ability to produce and test them. An advanced system integrating automated assembly and testing became an urgent priority, not only for increasing volume, but also
  • Medical Device Link .
    incorrectly." The advantage of achieving a waiver classification for assays is that labs with a waiver certificate can perform such assays. Since 63% of labs have a waiver certificate, an assay with waiver status can be sold to many more labs. The key difference between the proposed and previous waiver
  • Medical Device Link .
    Using specialty labs to develop IVDs Specialty labs offer IVD manufacturers expertise in standardization and generation of clinical utility data. Developing an IVD assay with broad utility as a routine clinical diagnostic requires numerous resources and skill sets. Since IVD manufacturers may lack
  • Medical Device Link .
    milliliters to microliters (and in some cases, nanoliters), with some test platforms using saliva, sweat, or urine to detect levels of analyte as low as picogram quantities. Advances in sample handling have also been important to assay improve ment. Reference labs such as Laboratory Corporation

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