INDIANAPOLIS, May 1, 2017 /PRNewswire/ -- Roche (SIX: RO, ROG;
OTCQX: RHHBY) announced today that its new, dedicated high-volume testing immunoassay solution for the cobas 8000 modular
analyzer series, the cobas e 801 module, has received 510(k) clearance from the U.S. Food and Drug Administration
(FDA).
As core laboratories continue to evolve to meet the growing workload demands in an increasingly challenging environment, the
cobas e 801 module offers greater testing efficiency, superior reagent management and industry-leading turnaround time for
critical diagnostic tests. Designed for maximum consolidation at a high throughput, the module reduces generated waste, for more
environmentally sustainable testing.
"The cobas e 801 module truly is a transformative solution," said Dr. Alan Wright, Chief
Medical Officer, Roche Diagnostics Corporation. "Patients and the physicians who serve them need medically relevant answers,
faster and with ever greater precision. This clearance delivers the instrumentation cornerstone of the next-generation lab—high
throughput, agility and intelligence."
The cobas e 801 module almost doubles the currently available immunoassay testing capacity on the same footprint,
delivering up to 300 tests per hour and providing 48 reagent channels.
Designed to use at least 25% less patient sample than its predecessor, the analyzer offers an extensive assay menu and
delivers speed, accuracy and consistency.
Advances that speed patient care
The cobas e 801 module is the newest member of the cobas 8000 modular analyzer series, delivering
immunoassay testing across a wide range of disease areas. Up to four cobas e 801 modules can be configured in a series,
delivering up to 1,200 tests per hour across up to 192 reagent positions. The system may also be integrated with the cobas
8100 automated workflow series and Roche Middleware featuring Lab Intelligence.
The cobas e 801 module allows for continuous, on-the-fly loading of reagents and consumables and has a high uptime,
while requiring less hands-on time. A new reagent pack design has increased reagent onboard stability to 16 weeks, allowing labs
to reduce send-out testing and minimize reagent waste.
The cobas e 801 module will continue to deliver Roche's industry-leading 9-minute STAT assays, allowing labs to reduce
turnaround time for critical testing, such as cardiac markers. The small sample volumes required for testing are beneficial for
patients, especially special populations like pediatrics and the critically ill.
About Roche
Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people's lives.
The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalized healthcare –
a strategy that aims to fit the right treatment to each patient in the best way possible.
Roche is the world's largest biotech company, with truly differentiated medicines in oncology, immunology, infectious
diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and
tissue-based cancer diagnostics, and a frontrunner in diabetes management.
Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable
contribution to society. The company also aims for improving patient access to medical innovations by working with all relevant
stakeholders. Twenty-nine medicines developed by Roche are included in the World Health Organization Model Lists of Essential
Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognized as the Group Leader
in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry eight years in a row by the Dow Jones
Sustainability Indices (DJSI).
The Roche Group, headquartered in Basel, Switzerland, is active in over 100 countries and in
2016 employed more than 94,000 people worldwide. In 2016, Roche invested CHF 9.9 billion in R&D
and posted sales of CHF 50.6 billion. Genentech, in the United
States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical,
Japan. For more information, please visit www.roche.com.
All trademarks used or mentioned in this release are protected by law.
For further information, please contact:
Christina Vysma
Communications Business Partner
Centralized Diagnostics
Roche Diagnostics Corporation
Indianapolis, Indiana USA
(317) 292.2920
christina.vysma@roche.com
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SOURCE Roche