MedMira Wins $4.2 Million U.S. Army Contract to Commercialize Rapid Triple Test
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MedMira Wins $4.2 Million U.S. Army Contract to Commercialize Rapid Triple Test

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MedMira Wins $4.2 Million U.S. Army Contract to Commercialize Rapid Triple Test PR Newswire HALIFAX, Nova Scotia, July 3, 2012 HALIFAX, Nova Scotia, July 3, 2012 /PRNewswire/ -- Under a US Army contract valued at USD$4.2 million, MedMira will develop and commercialize this multiple rapid test which detects HIV, Hepatitis B and C simultaneously in 3 minutes from a single drop of blood. (CNW Group/MEDMIRA INC.) MedMira Inc., (MedMira) (TSXV: MIR), a developer of rapid diagnostic technology and solutions, announced today that it has been awarded a U.S. Army Medical Research Acquisition Activity (USAMRAA) contract to develop and commercialize a rapid test capable of simultaneous detection of HIV and Hepatitis B and C. The contract, awarded through a competitive bid process, involves a two-year base period and a 10-month option with a value of USD$4,266,144, if all options are exercised. MedMira presented its technology and multiple rapid test, which met the U.S. Army's advanced technology readiness level requirements. The Multiplo Rapid HBV/HIV/HCV Antibody Test resulting from this contract award will be deployed on the frontlines of military healthcare for use in emergency screening for transfusion transmitted diseases where no FDA approved donor screening tests are available. The military could also put the test to use during pre and post deployment screenings and civilian disaster relief efforts.

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MedMira Wins $4.2 Million U.S. Army Contract
to Commercialize Rapid Triple Test
PR Newswire
HALIFAX, Nova Scotia, July 3, 2012
HALIFAX, Nova Scotia
,
July 3, 2012
/PRNewswire/ --
Under a US Army contract valued at
USD$4.2 million
,
MedMira will develop and commercialize this multiple
rapid test which detects HIV, Hepatitis B and C
simultaneously in 3 minutes from a single drop of
blood. (CNW Group/MEDMIRA INC.)
MedMira Inc., (MedMira) (TSXV: MIR), a developer of rapid diagnostic
technology and solutions, announced today that it has been awarded a U.S.
Army Medical Research Acquisition Activity (USAMRAA) contract to develop and
commercialize a rapid test capable of simultaneous detection of HIV and
Hepatitis B and C.
The contract, awarded through a competitive bid process, involves a two-year
base period and a 10-month option with a value of
USD$4,266,144
, if all options
are exercised. MedMira presented its technology and multiple rapid test, which
met the U.S. Army's advanced technology readiness level requirements. The
Multiplo Rapid HBV/HIV/HCV Antibody Test resulting from this contract award
will be deployed on the frontlines of military healthcare for use in emergency
screening for transfusion transmitted diseases where no FDA approved donor
screening tests are available. The military could also put the test to use during
pre and post deployment screenings and civilian disaster relief efforts.
"We are thrilled to receive this new contract from USAMRAA for the
development and commercialization of our Multiplo test. This contract award
demonstrates the excellent fit between MedMira's technology and products and
military requirements. We have built a lasting relationship with the U.S. Army,
delivering advanced diagnostic solutions that reduce the need for militaries to
undertake ground-up development work," said Hermes Chan, CEO, MedMira
Inc. "MedMira's technology and products are elegantly simple, portable, fast,
and high quality. All of these attributes are mission critical in deploying
diagnostic healthcare solutions on the frontlines of military healthcare."
Chan continued, "Our team recently attended a conference focused on military
pre-hospital trauma management where we heard first hand of the need for a
multiple rapid HBV/HIV/HCV test from many of the leading experts, military
personnel, and medical professionals in this field."
Under contract number W81XWH-12-C-0151 the U.S. Army will fund all
development costs and associated fees in obtaining a U.S. Food and Drug
Administration (FDA) premarket approval (PMA) for this multiple rapid test. The
scope of work under this contract will see MedMira advance and fully
commercialize a multiple rapid test that will simultaneously detect three of the
most serious infectious diseases, namely HIV-1/2, Hepatitis B, and C antibodies
within three minutes using just a small drop of blood. Once approved, the
product will be supplied by MedMira directly to the U.S. Army and to other
customers throughout the world, both military and civilian, via the Company's
distribution network.
"
A multiplexed test for transfusion transmitted diseases provides an enabling
technology that will be used to mitigate risk in austere environments where
emergency blood collections are necessary to save lives of severely wounded
war fighters," said Colonel Richard Gonzales, Product Manager, U.S. Army
Medical Materiel Development Activity.
About MedMira
MedMira is a leading developer and manufacturer of flow-through rapid
diagnostics and technologies. The Company's tests provide hospitals, labs,
clinics and individuals with reliable, rapid diagnosis for diseases such as HIV and
hepatitis C in just three minutes. The company's tests are sold under the
Reveal®, Multiplo™ and Miriad brands in global markets. MedMira's rapid flow-
through HIV test is the only one in the world to achieve regulatory approvals in
Canada
,
the United States
,
China
and the European Union. MedMira's corporate
offices and manufacturing facilities are located in
Halifax, Nova Scotia
, Canada.
For more information visit MedMira's website at http://www.medmira.com.
This news release contains forward-looking statements, including statements
relating to growth in the Company's business, earnings and profitability, and
trends in demand for the Company's products, which involve risk and
uncertainties and reflect the Company's current expectation regarding future
events including statements regarding possible future growth and new business
opportunities. Actual events could materially differ from those projected herein
and depend on a number of factors including, but not limited to, changing
market conditions, successful and timely completion of clinical studies,
uncertainties related to the regulatory approval process, establishment of
corporate alliances and other risks detailed from time to time in the company
quarterly filings.
Neither TSX Venture Exchange nor its Regulation Services Provider (as that
term is defined in the policies of the TSX Venture Exchange) accepts
responsibility for the adequacy or accuracy of this release.
For further information:
MedMira Contact:
Andrea Young, Corporate Communications
Tel: +1-902-450-1588
Email: ayoung@medmira.com
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