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

Download Mobile App




Calbiotech Awarded Contract to Develop Reagents for Dengue Diagnosis

By LabMedica International staff writers
Posted on 24 Nov 2009
A Small Business Innovative Research (SBIR) Phase I contract by the U.S. More...
Army Medical Research and Material command has been awarded to Calbiotech (Spring Valley, CA; USA), which will develop analyte specific reagents (ASRs) for the diagnosis of Dengue virus.

Technology developed under this project will enable an affordable FDA approved method for diagnosing Dengue fever in blood/sera. This will enable medical personnel to adequately diagnosis and react to Dengue fever outbreaks.

Dengue virus is a mosquito born species of Flavivirus that represents a major threat to military forces deployed to tropical areas of the world. Due to its worldwide distribution, US military and civilian personnel deployed overseas are at high risk of being infected. The global prevalence of Dengue has grown dramatically in recent decades, spreading from 9 to some 40 countries. The disease is now endemic in more than 100 countries in Africa, the Americas, the Eastern Mediterranean, South-East Asia, and the Western Pacific. Not only is the number of cases increasing as the disease is spreading to new areas, but explosive outbreaks are occurring. In 2007, Venezuela reported over 80,000 cases.

This Phase I award will allow Calbiotech to compete for $730,000 in Phase II funding. A Phase II project would expand the work to develop ASRs for Rift Valley fever, Sand Fly fever-Toscana, Crimean-Congo fever, Central European Tick-borne encephalitis, and Chikungunya virus in blood/sera from clinically ill patients.

Calbiotech provides preclinical and research testing services for testing human and animal samples using the Calbiotech Immunoassay menu. Calbiotech is FDA registered and ISO 13485:2003 certified facility. The company has adopted operating polices based on FDA Quality system (QS), current Good manufacturing Practices (cGMP), Good laboratory Practices (GLP) and ISO requirements, EU directive and Canadian medical devices regulations.

Related Links:
Calbiotech


Gold Member
Collection and Transport System
PurSafe Plus®
POC Helicobacter Pylori Test Kit
Hepy Urease Test
Gold Member
Immunochromatographic Assay
CRYPTO Cassette
Gold Member
Hybrid Pipette
SWITCH
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

Hematology

view channel
Image: Residual leukemia cells may predict long-term survival in acute myeloid leukemia (Photo courtesy of Shutterstock)

MRD Tests Could Predict Survival in Leukemia Patients

Acute myeloid leukemia is an aggressive blood cancer that disrupts normal blood cell production and often relapses even after intensive treatment. Clinicians currently lack early, reliable markers to predict... Read more
Copyright © 2000-2026 Globetech Media. All rights reserved.