Corporate News | ARUP Laboratories
WEBAug 20, 2024 · ARUP to Host House Ways and Means Committee Field Hearing on Healthcare Innovation. ARUP Laboratories has been chosen as the site for a House Ways and Means Committee Field Hearing on July 12. Topics include medical innovation, healthcare access, and economic prosperity.
FDA Approves ARUP Laboratories' AAV5 DetectCDx™, a First …
WEBJun 30, 2023 · AAV5 DetectCDx ™, which was developed by ARUP Laboratories in collaboration with BioMarin, is the first companion diagnostic immunoassay for a gene therapy product to receive FDA approval.
New ARUP Laboratories' Grant Will Fund Innovative Research to …
WEBJul 30, 2024 · The new grant will fund cutting-edge research in laboratory medicine that has the potential to significantly impact patient care. The research grant is named in honor of retired ARUP CEO...
ARUP's New Institute for Research and Innovation in Diagnostic …
WEBSep 29, 2023 · ARUP Laboratories today announced the formation of the new ARUP Institute for Research and Innovation in Diagnostic and Precision Medicine™ (R&I Institute).
Press Releases | ARUP Laboratories
WEBARUP Laboratories Urges FDA to Withdraw Proposed Rule Regulating Laboratory-Developed Tests. ARUP believes the FDA’s plan to regulate lab-developed tests will limit access to testing, increase costs, and face a court challenge, and is calling for collaboration to better address LDT oversight.
ARUP Laboratories Urges FDA to Withdraw Proposed Rule …
WEBNov 29, 2023 · ARUP Laboratories today released the company's public comment on the FDA's proposed rule to regulate laboratory-developed tests (LDTs) as medical devices, urging the agency to withdraw the rule.
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Newsroom - ARUP Laboratory
WEBSep 3, 2024 · Explore the ARUP Newsroom Stay informed about the latest from ARUP. Explore press releases, news articles, our Magnify publication, and more.
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ARUP Statement on FDA Final Rule to Regulate ... - ARUP Laboratories
WEBApr 29, 2024 · SALT LAKE CITY—A final FDA rule regulating laboratory-developed tests (LDTs) as medical devices does not address serious concerns raised by ARUP Laboratories and the clinical laboratory community, and the company’s stance on the rule has not changed, CEO Andy Theurer said today.
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