Six Sigma Can Help Monitor New CLIA Proficiency Testing Changes
A PT update went into effect on January 1, focusing on revised acceptance limits, among other modifications
Lab Compliance Advisor
Practical, “What-to-Do” and “How-to-Do-It” Help to Comply with the Latest State & Federal Laws, Rules & Regulations that Affect Your Diagnostic Lab or Pathology Practice
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Articles and Reports
Compliance Concerns: Laboratory Regulations in 2024 and Beyond
Earle S. Collum, chair of the CAP Council on Accreditation, talks through regulatory changes in 2024 and what to expect from 2025
2024 Laboratory Reimbursement Trends and What to Expect in 2025
Revenue cycle management experts weigh in on the biggest developments of 2024 and how labs can best prepare for 2025 and beyond
Tennessee Pain Doctor Faces Jail for Opioid Abuses, Medicare Fraud
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Labs In Court: A roundup of recent cases and enforcement actions involving the diagnostics industry
From - Lab Compliance Advisor
Case: A new DOJ lawsuit accuses a West Virginia non-profit hospital and its business consultant of seeking to dominate the Ohio Valley market by…
Pain Management Clinic, 2 MDs Pay $99K to Settle Millennium Free POCT Cup Kickback Claims
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OIG Monthly Work Plan Review: April 2019
From - Lab Compliance Advisor
Among the 10 new Work Plan items this month, three may have potential ramifications for at least some labs…
Texas Pathology Lab Settles EHR Consulting Kickback Claims for $63.5 Million
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Case of the Month: Another MD-Owned Lab Gets Busted for Urine Drug Test Abuses
From - Lab Compliance Advisor
Fraudulent utilization and billing of urine drug screening first became a priority for federal enforcers since the…
Mass. Pain Management MDs Jailed for Elaborate Drug Testing Conspiracy
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Compliance Perspectives: How the New OIG Fraud Risk Indicator System Heightens the Imperative of Self-Disclosure
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Lab Settles Specimen Collection Fee Kickback Charges for $2.275 Million
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FDA Extends Deadline to Comment on Proposed 510(k) Pathway Reform
From - Lab Compliance Advisor
April 22, 2019 was supposed to the last day to comment on newly proposed FDA guidance on changing the Section 510(k) premarket review process for…