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BioWorld - Tuesday, March 31, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Sep. 30, 2014

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FDA said to have reclaimed role of 'leading arbiter' of ad, promo policy

WASHINGTON — The Affordable Care Act torqued the statute on qui tam lawsuits in important ways, which is one of several factors that have placed substantially greater influence in the hands of agencies other than FDA over FDA-regulated communication. However, Jennifer Bragg, a partner at Skadden, Arps, Slate, Meagher & Flom (New York) told an audience here in the nation's capital that FDA is paying far more attention to such issues for a number of reasons, and thus, "I believe FDA has reclaimed its role of the leading arbiter of policy" in this area. Read More

Latin America: Dominican Republic boosts position as a strategic med-tech manufacturer

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Inside The Beltway: FDA clears Single-Site wristed device for use with Intuitive's da Vinci system

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Google Glass: Researchers ask if Google Glass is next big thing for healthcare

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World In Review: CVRx gets Ireland approval for the Barostim neo system

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Acreements/contracts: OSI, CIS form collaboration to reach out to oncology facilities

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People in Places

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Hit Bits: AliveCor launches new version of AliveECG app for AF detection

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Patents: PMT receives two patents forcervical distraction, joint implants

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Briefly Noted

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product briefs

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MDD's Cardiology

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