Fighting the FDA’s Final Rule on LDTs
CEO Laurie Menser discusses the Association for Molecular Pathology’s court case against the FDA’s rule on laboratory-developed tests.
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Getting Started with the FDA’s New LDT Rule
Experts explain what the phase-in process will look like—and how labs can get ahead of the game.
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Transitioning the Clinical Lab
What clinical laboratory professionals need to know about healthcare provision for transgender and nonbinary patients
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Mayo Clinic to Shut Down New England Laboratory
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FDA Intervenes on Development of New Zika Test
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Accumen Acquires Chi Solutions to Expand Laboratory Management, Consulting Business
From – Laboratory Industry Report
Accumen, Inc. (San Diego) specializes in “healthcare transformation,” and now the company is transforming itself by joining forces with Chi Solutions (Ann Arbor, Mich.) to expand its clinical laboratory management and…
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ACLA Pushing for Broadening of Coverage for Vitamin D Testing
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CAP Issues New Guidelines for Reports on Bone Marrow Testing
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Neoteryx–A Less Ambitious Version of Theranos?
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FDA Issues Informational Queries to Two Startup Labs
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Smaller Publicly-Traded Labs Report Mixed Results
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Veritas Launches Below-$1,000 Whole Genome Test
From – Laboratory Industry Report
Veritas Genetics is launching a whole genome test under the four-figure price point…
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