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Monday, September 08, 2008

"The ARTEL MVS is recognized by many of our customers and is used in their own labs. It is an industry standard so our customers know they are comparing apples-to-apples when they see our results. The MVS provides us with non-subjective data that builds credibility with our customers."

 

Director of Applications

Pipette / Auto Equipment Manufacturer

 


Liquid Handler Performance Verification Service


 

Liquid Handler Performance Verification ServiceAs part of the LHQA™ suite of services, ARTEL provides on-site, third party volume transfer performance assessment for most makes and models of automated liquid handling systems. 

For a custom quote for Liquid Handler Performance Verification Services, please contact ARTEL at 888-406-3463 or email at orders@artel-usa.com.

 

Benefits

  • Documented performance results that are traceable to the National Institute of Standards and Technology (NIST)
  • Use of the MVS, a standardized volume verification system, to ensure repeatability of liquid handler methods between laboratories or locations for improved liquid handling quality assurance
  • Precision and accuracy assessment for all tips
  • Tip-by-tip and well-by-well statistics for volumes transferred into 96-well or 384-well microtiter plates
  • Execution of the volume transfer measurements for your laboratory so you can focus on your work
  • Standardized and customized volume transfer assessment services to assist with performance qualification (PQ) requirements
  • Dilution step accuracy determination for dilutions up to 1:2048 of the starting material 
  • Non-aqueous solution volume transfer analysis to identify variances associated with liquid class properties

 

Examples of LHQA Usage

  • Volume transfer performance assessment for scheduled or periodic services for liquid handlers in one or more laboratories or locations
  • Site acceptance testing of new equipment, or of dormant equipment prior to being brought back on-line
  • Demonstration of liquid handler performance to colleagues, customers, or interested parties in a fast, reliable way
  • Facilitation in writing operating procedures and methods for assays
  • Compliance with internal documentation
  • Post repair/maintenance checks of equipment before running an assay
  • Periodic diagnostic testing of equipment to ensure accuracy and precision on a well-by-well and/or tip-by-tip basis
  • Frequent, quick volume checks (interim performance checks) as a method is being optimized
  • Evaluation of new volume transfer strategies, i.e., to show cause-and-effect volume-based measurements after manipulations to method parameters or liquid class settings (reverse mode pipetting vs. forward mode, air gap use, tip touches, dispense rates/heights, wet dispense vs. dry dispense, etc.)
  • Side-by-side comparison of dispensed volumes (performance checks) between one or more automated methods and/or one or more liquid handlers (method-to-method or device-to-device comparisons)
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