Agilent Unveils Biopharma CDx Services Lab to Accelerate Precision Medicine
09 Settembre 2024 - 2:00PM
Business Wire
New CLIA-certified lab ensures seamless transition from early
assay development and testing to full companion diagnostics
commercialization
Agilent Technologies Inc., (NYSE: A) today announced the launch
of its Biopharma CDx Services Lab (BCSL) in Carpinteria,
California, following receipt of California State clinical
laboratory license and Clinical Laboratory Improvement Amendments
(CLIA) certificate of compliance.
These credentials signify that the lab operates in accordance
with CLIA regulations, which are federal standards applicable to
all U.S. facilities testing human specimens for health assessment,
diagnosis, prevention, or treatment of diseases. The CLIA
certificate of compliance ensures high standards for accuracy and
reliability in laboratory testing, confirms regulatory adherence,
boosts market credibility, and improves operational efficiency.
The BCSL and Agilent’s assay development model will support drug
development from early clinical studies through regulatory approval
with efficient, flexible, and streamlined companion diagnostic
development. The BCSL will also provide access to innovative
technologies for biomarker assessment with novel precision
therapeutics in clinical trials, as well as high-quality assays
that deliver robust data. The continuous development model from
feasibility through FDA approval of companion diagnostics offers
significant cost and time advantages to biopharma seeking to
maximize the value of their investment in companion diagnostics and
precision therapeutics.
“Agilent is committed to advancing the frontiers of biopharma
and clinical diagnostics. The launch of the Biopharma CDx Services
Lab represents a significant milestone in the company’s mission to
support the development of innovative therapeutics and precision
medicine,” stated Nina Green, vice president and general manager of
Agilent’s Companion Diagnostics (CDx) Division. “By providing
cutting-edge technologies and high-quality assays, Agilent aims to
streamline the path from early clinical studies to FDA approval,
accelerating the delivery of life-changing treatments to
patients.”
Launching the BCSL is a key element in Agilent’s broader
strategic commitment to the biopharma, clinical diagnostics, and
precision medicine sectors. It strengthens the company’s
capabilities in early assay development, technology innovation, and
prospective clinical trial patient testing, while underscoring
Agilent’s dedication to being a trusted partner in the biopharma
industry and shaping the future of healthcare.
About Agilent Technologies
Agilent Technologies Inc., (NYSE: A) is a global leader in
analytical and clinical laboratory technologies, delivering
insights and innovation that help our customers bring great science
to life. Agilent’s full range of solutions includes instruments,
software, services, and expertise that provide trusted answers to
our customers' most challenging questions. The company generated
revenue of $6.83 billion in fiscal 2023 and employs approximately
18,000 people worldwide. Information about Agilent is available at
www.agilent.com. To receive the latest Agilent news, please
subscribe to the Agilent Newsroom. Follow Agilent on LinkedIn and
Facebook.
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Naomi Goumillout Agilent Technologies +1.978.314.1862
naomi.goumillout@agilent.com
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Da Gen 2024 a Gen 2025