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New Technology Reduces Risk of IVF Laboratory Mistakes by Electronically Identifying Sperm, Eggs and Other Materials for Each Patient
Date:11/12/2009

CORNWALL, England, Nov. 12 /PRNewswire/ -- A new software technology is helping to reduce the risk of laboratory errors in infertility treatment, by electronically identifying the sperm, eggs, resulting embryos and other materials used in in vitro fertilization (IVF) treatment cycles. Using non-invasive Radio Frequency Identification (RFID), IVF Witness(TM) can track a patient's sperm, eggs and embryos during the course of treatment. If the wrong material is introduced in the lab environment, IVF Witness alerts the staff, via visual and audible signals, to help prevent mislabeling of any materials.

While laboratory errors are rare, by creating an automated system to minimize the chance for mix up, IVF Witness safeguards the infertility treatment process and gives patients peace of mind.

The IVF Witness is being used in infertility clinics worldwide, including leading clinics in the UK and United States. Since launching this new technology last year, over 20,000 infertility treatment cycles have employed IVF Witness to ensure the safety and security of patients' genetic material.

IVF Witness uses RFID tags, each containing a microchip that acts as a unique digital fingerprint, safely identifying samples at the outset and tracking them through the fertilization process. Each patient is given an RFID identity card, with a unique identification, that are used with all sample materials for that patient, including Petri dishes and test tubes used in a patient's treatment cycle. The entire system is electronically managed.

"Our aim was to develop a system that automatically tracks a patient's eggs, sperm and resulting embryos during an infertility treatment cycle, to reduce the risk of mislabeling or error," said Bill Brown, President of Research Instruments. "Infertility treatment is a very precise and personal process and IVF Witness helps to maintain the integrity and security of this process for both healthc
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SOURCE Research Instruments
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