The Dark Report Archives

Global Computer Outage Shows Risk to Clinical Labs

CEO SUMMARY: Last Friday’s global computer outage was due to a faulty update to a widely used endpoint security software system. The level of disruption worldwide in air travel, commerce, and information processing was unprecedented. This incident highlights that there are risks when a clinical laboratory or hospital puts both data and services in the […]

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Language in Draft House Bill Directs FDA to Suspend LDT Rule

Laboratory Compliance / Robert Michel

THERE IS AN INTERESTING NEW DEVELOPMENT associated with the regulation of laboratory developed tests (LDTs) by the Food and Drug Administration (FDA). In recent days, a House committee published draft legislation that directs the FDA to suspend its implementation of the LDT rule. As part of an appropriations bill, the House Appropriations Committee issued a

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2023 Ranking of the World’s Top 13 IVD Corporations

In Vitro Diagnostics / Robert Michel

BASED ON 2023 DIAGNOSTICS-RELATED REVENUE, four in vitro diagnostics (IVD) manufacturers continued to lead the global IVD market just as they did in 2022. They are: Thermo Fisher Scientific, Inc., Roche Holdings, Abbott Laboratories, and Danaher Corporation. The top 13 firms collected $88.7 billion in annual revenue, compared to $99 billion in fiscal 2022 and

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Labs, Payers Don’t Like Prior Authorization for Genetic Tests

Managed Care Contracts / Robert Michel

EDITOR’S NOTE: Our column, Virchow, is written by anonymous insiders working within the managed care world. The column aims to help clients of The Dark Report better understand the decisions, policies, and actions of payers as they manage their laboratory networks, establish coverage guidelines, process lab test claims, and audit labs. Prior authorization requirements for genetic

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What Labs with LDTs Must Do to Comply with FDA’s LDT Rule

Laboratory Compliance / Robert Michel

CEO SUMMARY: Until the recently filed court challenge to the Food and Drug Administration’s LDT rule succeeds or Congress intervenes with new legislation, those clinical laboratories performing laboratory developed tests (LDTs) must comply with the requirements of the new rule. This compliance will require substantial staff time and costs that may outweigh the benefit to

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Quest Diagnostics Moves to Acquire LifeLabs of Canada

Laboratory Management / Robert Michel

QUEST DIAGNOSTICS, ALREADY A CLINICAL LABORATORY BEHEMOTH IN THE U.S., is expanding its North American footprint by acquiring Canada’s largest independent laboratory company. Quest Diagnostics announced on July 3 that it had a “definitive agreement” to acquire LifeLabs from the Ontario Municipal Employees Retirement System (OMERS) in a deal valued at approximately $1.35 billion in

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Invitae’s Troubled Journey: Rise, Fall, and Bankruptcy

Genetic Testing / Robert Michel

ON MAY 7, THE REMNANTS OF GENETIC TESTING GIANT INVITAE (NYSE: NVTA) were scooped up by Labcorp when the United States Bankruptcy Court approved Labcorp’s bid to acquire Invitae’s assets. Labcorp will receive “select assets of Invitae on a going concern basis for $239 million in cash consideration, plus other non-cash consideration,” PR Newswire noted.

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July 22, 2024, Intelligence: Late-Breaking Lab News

Late Breaking Lab News / Robert Michel

Some hospitals failing to comply with the federal price transparency regulation have been fined. The website of CMS.gov lists 15 hospitals and the amount each was fined. On June 6, 2022, the first fines were levied against Northside Hospital of Atlanta ($883,130) and Northside Hospital Cherokee of Canton, Ga. ($214,320). On Feb. 27, 2023, UF

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New Type of Competition from Investor-Owned Labs

Clinical Laboratory Trends / Robert Michel

CEO SUMMARY: More investor-funded lab companies see robust future growth in serving what The Washington Post calls “a booming online wellness market that aims to leave the doctor’s office behind. ” This is a new market driven by younger health care-minded consumers who turn to the web for information and resources without first speaking with

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Clarapath Automates Slide Prep, Microtomy Workflow

Anatomic Pathology, Uncategorized / Robert Michel

>>CEO SUMMARY: Histology is one area of laboratory medicine that utilizes a mostly manual work flow. However, pathology labs will soon have a novel solution designed to automate many of the steps in microtomy that produce glass slides. Reduced variability in the finished glass slides can improve the scanning process, thereby generating better quality whole

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