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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Four Federal Efforts to Monitor, Including RESULTS Act Progress
Other proposals aim to increase fraud enforcement, temper prior authorization, and modernize CLIA
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PAMA Delay Proposed Until 2027 Under a New Federal Spending Bill
However, attorney Danielle Sloane urges labs to be proactive about potential PAMA reporting requirements on Jan. 31 if the bill doesn’t pass quickly
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Congress Nearing Deadline for Medicare ‘Doc Fix’
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Reaction Split on New Changes to Clinical Laboratory Fee Schedule
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Industry Groups Applaud New CBO Score On Closing Stark Loophole
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Pathologists Exempt From 2015 Meaningful Use Penalty
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Massachusetts Targets Self-Referral of Laboratory Services
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Congress Passes Continuing Resolution, Heads Home Until November
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‘Doc Fix’ Legislation Estimated to Cost $144B Over 10 Years
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