Capture of the exact timing of add-on orders relative to initial specimen collect was only possible with the new LIS (August 2, 2014 – December 31, 2014; complete data available on 56,389 add-on ...
The US Food and Drug Administration is proposing to step up its oversight of a growing category of medical tests called laboratory-developed tests. The FDA approves and clears many types of lab tests ...
As the year comes to a close, the government has signaled a specific focus on clinical laboratories for 2023. On December 6, 2022, the U.S. Department of Health and Human Services Office of the ...
The Eliminating Kickbacks in Recovery Act (EKRA) was enacted by Congress in October of 2018 as part of the SUPPORT Act. 1 While its initial focus was to address patient brokering and kickback schemes ...
Expertise from Forbes Councils members, operated under license. Opinions expressed are those of the author. One of the most rapidly accelerating health trends today is direct-to-consumer lab testing, ...
Genetic testing that reveals potential cancer risks or other maladies with no regulatory oversight is among the targets of the agency’s proposed review. By Christina Jewett The Food and Drug ...
Estimated hours per day of manual effort for add-on testing prior to introduction of robotic archival storage/retrieval unit 30.7 Estimated hours per day of manual effort for add-on testing with use ...
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