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BioWorld - Sunday, May 5, 2024
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BioWorld MedTech
Oct. 21, 2014
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MedTech Forum: Halftime over, EU restarts its contentious CE regulation talks
BRUSSELS, Belgium — For those concerned about the revision of rules governing the popular CE mark for commercializing medical devices in Europe, let's say we are somewhere in the third quarter.
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MedTech Forum: CE Mark revision: 'We do not want device scrutiny by lottery'
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Veracyte developing new test to remove ambiguity from ILD screening
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Inside the Beltway: AHRQ survey; multiple chronic conditions still driving spending
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Financings: PureTech closes $55 million growth stage investment round
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Hit Bits: Toledo Clinic & Outpatient Center selects eClinicalWorks EHR solution
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Agreements/contracts: Mediso launches new MRI with new Tesla strength
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People in Places
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World in Review: MedVenture reports expansion of its operations into Costa Rica
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Product briefs
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MDD's Cardiology Extra
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