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. Read More

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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