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BioWorld - Tuesday, February 10, 2026
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BioWorld MedTech
March 31, 2011
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Panel gives insight on FDA in development process
ATLANTA – What happens when you put a former FDA reviewer, a CEO who's product failed to garner approval in the U.S., and a researcher, who helps companies navigate the regulatory space in the same room? (Medical Device Daily)
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Concerns raised about trends in the teleradiology industry
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International report: EDAP to sell MMS urodynamic diagnostic products in Japan
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Washington roundup: Industry sees double-dipping in IRS device tax regulation
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Deals roundup: Align to 'streamline' procedure with $190M Cadent purchase
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MDD
's food for med-tech thought
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People in the News
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Med-Tech Notes
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