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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

July 29, 2011

View Archived Issues

Look for unusual suspects when detecting glucose monitor errors

ATLANTA – Back in 2010, the FDA held two meetings to discuss the accuracy and safety of glucose meters. During the meetings the agency pushed for tightening system accuracy criteria specified by current glucose meter standards and considered whether FDA review criteria for these devices should be changed to promote the public health. The FDA solicited feedback from clinical experts about the clinical requirements for blood glucose meter accuracy and precision, and the benefits and risks of using glucose meters to achieve and maintain tight glycemic control. (Medical Device Daily) Read More

New clinical research validates Calypso's Gating technology

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Report from Europe: Varian awarded Scottish hospital contract for TrueBeam system

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Washington roundup: Senate HELP committee shows ideological divide on user fees

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Financings roundup: Boston Sci to buy back up to $1B of its stock

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MDD's food for med-tech thought

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New ventures: Baxter forms early-stage ventures unit, plans to invest up to $200M

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Agreements/contracts: SCOA selects Cardinal's VitalSource as GPO

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People in the News

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HIT roundup: Cottage Hospital meets MU criteria with HMS EHR

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Product Briefs

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MDD's Diagnostic Extra

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