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CARES Act
Payers Request More Claims Documentation
By Robert Michel | From the Volume XXX, No. 7 – May 8, 2023 Issue
CEO SUMMARY: Both anecdotal evidence from lab professionals and numbers-based data from XiFin point to a problem: More payers require clinical labs to produce more documentation that a test claim i…
To Stay Afloat, Dallas AP Group Cut Staff, Payroll
By Joseph Burns | From the Volume XXVII No. 7 – May 11, 2020 Issue
CEO SUMMARY: As early cases of COVID-19 spread inĀ some states, pathologists at the 50-member ProPath group inĀ Dallas prepared for a widespread outbreak by preserving cashĀ and working with bankers and other advisors to apply for federalĀ stimulus funding. Executives also fur…
Labs May Qualify for Relief Under New Federal Laws
By Joseph Burns | From the Volume XXVII No. 6 – April 20, 2020 Issue
CEO SUMMARY: After routine testing and specimen volumeĀ declined last month, so too did the associated revenue. InĀ response, clinical laboratories and anatomic pathology groupsĀ want to bolster their finances quickly or risk incurring moreĀ financial damage to already-fragile…
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Volume XXXI, No. 10 – July 22, 2024
An attorney widely experienced in clinical laboratory regulation has prepared guidelines for complying with the FDA’s new LDT rule, and The Dark Report offers them in their entirety to readers. Also, a House of Representatives bill includes language calling for the FDA to suspend its rule.
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