ARUP Laboratories has filed a declaration supporting a lawsuit against the FDA brought by the American Clinical Laboratory Association. |
May 30, 2024 |
ARUP Files Declaration to Support Lawsuit Challenging the FDA's Rule to Regulate Lab-Developed Tests ARUP’s declaration amplifies the lawsuit’s claims that the FDA does not have legal authority over laboratory testing services and that regulating these services is unreasonable. |
Jonathan Genzen, MD, PhD, ARUP’s chief medical officer and senior director of governmental affairs, and Jonathan Carr, JD, chief compliance officer, discuss the FDA’s final rule on LDTs. |
May 28, 2024 |
ARUP Webinar on the FDA’s Final Rule on Laboratory-Developed Tests Now Available ARUP Laboratories is committed to helping clients and the clinical laboratory community navigate regulatory changes and is offering current resources and a new webinar. |
David Shiembob, MBA, C(ASCP)CM, manager of ARUP Healthcare Advisory Services, has received the Clinical Laboratory Scientist Achievement Award from the Association for Diagnostics and Laboratory Medicine (ADLM). |
May 21, 2024 | ARUP Healthcare Advisory Services Manager David Shiembob has received the ADLM Clinical Laboratory Scientist Achievement Award, which recognizes significant contributions to the CLS community. |
Erica Clyde speaks with attendees at BioHive Live. |
May 10, 2024 | The inaugural event created connections among future innovators who look to solve many of healthcare’s biggest challenges. |
May 9, 2024 |
Special 40th Anniversary Edition of ARUP’s Magnify Magazine Now Available Online This issue highlights milestones in ARUP’s history, gives a glimpse into the company’s future, and includes a special feature: a video of ARUP founders and current leaders reminiscing and celebrating. |
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ARUP maintains that the FDA’s rule will limit access to testing, stifle innovation, and increase healthcare costs. |
April 29, 2024 |
ARUP Statement on FDA Final Rule to Regulate Laboratory-Developed Tests as Medical Devices ARUP maintains that the FDA’s rule will limit access to testing, stifle innovation, and increase healthcare costs. |