Software as a Medical Service, or SaMS, Takes Spotlight in New CMS Proposal
Clinical labs have until Aug. 31 to submit public comments about the anticipated changes
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New Enhancing CLIA Act: What Lab Directors Need to Know
The proposal seeks to move any future LDT authority away from the FDA
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How to Stay Ahead of Anticipated CLIA Deficiencies
Consultant Nora Hess offers suggestions for clinical labs to navigate these problems
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Evaluate, increase your lab’s compliance budget
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Congress Asks CMS to Delay PAMA Implementation
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OIG Releases 2016 Work Plan, Again Targeting Laboratory Billing
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FDA and CMS Address LDT Regulation Before Energy and Commerce Committee
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News at a Glance – Sep 2015
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Latest Fraud Takedown and CMS Fraud Detection Strategies Yield Big Returns
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AG’s Office Offers Compliance Tips While Noting New Enforcement Strategies
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Outcome of LDT Regulation Controversy Defies Forecasting
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News at a Glance – Jul 2015
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