We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress hp
Sign In
Advertise with Us
Vicotex

Download Mobile App




Leukemia Fusion Genes Screening Kit Gets CE IVD Status

By LabMedica International staff writers
Posted on 16 Jun 2015
The Leukemia Fusion Genes screening kit has been released as a Conformité Européenne In Vitro Diagnostic (CE-IVD) product under the European Directive for In Vitro Diagnostic Medical Devices.

The screening kit provides a sensitive, specific, reliable and cost-effective tool that is easy to perform for the routine screening of leukemia fusion transcripts. More...
The ability to detect cancer specific fusion genes is important in clinical settings to ensure that correct diagnosis is made and the optimal treatment is chosen.

Leukemia Fusion Genes (Q30) Screening Kit (QuanDx Inc.; San Francisco, CA, USA) is a qualitative in vitro diagnostic device for use in a clinical laboratory for the simultaneous detection of 30 fusion genes utilizing a novel multiplex reverse transcription real-time polymerase chain reaction (PCR) system. Fusion and control gene transcripts are co-amplified in each reaction and identified by specific fluorescent probes. Leukemia Fusion Genes (Q30) will transform current testing to provide a more efficient and economical system for optimizing patient testing as current methodologies to detect such fusion genes all have distinct shortcomings. The results of the test are ready in two to three hours.

Matthew Lei, PhD, Chief Executive Officer of QuanDx Inc., said, “This marks another significant step for our company and compliments our ISO 13485: 2003 certification in March. We have implemented the internal quality and regulatory processes necessary to move from selling a research use only product to an in vitro diagnostic product. CE marking demonstrates our commitment to provide quality diagnostic products to the European market. This is our first in vitro diagnostic product. The release of our CE marked product line is expected to expand the use of our assays for the identification of fusion genes in hematologic malignancies.”

Graeme Duncan, Vice President of Sales and Marketing at QuanDx, commented: “The CE marked Leukemia Fusion Genes product will be available in the European market beginning June 2015. The CE mark assures laboratories and clinicians that they can rely on Leukemia Fusion Genes Screening Kits to provide accurate results in their assessment and classification of hematological malignancies. The CE-IVD status of this Leukemia Fusion Genes (Q30) Screening Kit allows us to continue to expedite our plans to enter the clinical market in Europe in what is a key area of growth outside the USA.”

Related Links:

QuanDx Inc. 



Platinum Member
Automated Coagulation Analyzer
Hemolumi H6
Gold Member
Automatic Hematology Analyzer
CF9600
LAIR2 Antibody Pair Set
LAIR2 Antibody Pair [Biotin]
POC Immunoassay Analyzer
Procise DX
Read the full article by registering today, it's FREE! It's Free!
Register now for FREE to LabMedica.com and get access to news and events that shape the world of Clinical Laboratory Medicine.
  • Free digital version edition of LabMedica International sent by email on regular basis
  • Free print version of LabMedica International magazine (available only outside USA and Canada).
  • Free and unlimited access to back issues of LabMedica International in digital format
  • Free LabMedica International Newsletter sent every week containing the latest news
  • Free breaking news sent via email
  • Free access to Events Calendar
  • Free access to LinkXpress new product services
  • REGISTRATION IS FREE AND EASY!
Click here to Register








Channels

Clinical Chemistry

view channel
Image: New findings demonstrate that anti-Müllerian hormone (AMH) may help identify which breast cancer patients are most likely to benefit from chemotherapy plus endocrine therapy (Image Credit: Shutterstock)

AMH Test Helps Predict Adjuvant Chemotherapy Benefit in Premenopausal Breast Cancer

Hormone receptor-positive, human epidermal growth factor receptor 2-negative (HR+/HER2-) breast cancer can present a difficult treatment decision in premenopausal patients with low recurrence scores.... Read more

Molecular Diagnostics

view channel
Image Credit: iStock

Sequencing-Based Newborn Screening Identifies Pediatric Cancer Risk at Birth

Newborn screening in the United States relies on heel-stick blood spots to identify rare, treatable disorders through biochemical testing, but these programs generally do not assess inherited cancer risk... Read more

Microbiology

view channel
Image: The QIAstat-Dx BCID GPF Plus AMR Panel is the first QIAstat-Dx panel for bloodstream infections to receive FDA clearance (Photo courtesy of Qiagen)

FDA Clears One-Hour Panel for Bloodstream Infection and AMR Detection

Bloodstream infections can rapidly progress to sepsis, a life-threatening condition affecting an estimated 1.7 million adults in the U.S. each year. Rapid identification of pathogens and antimicrobial... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.