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BioWorld - Wednesday, December 31, 2025
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

June 2, 2011

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Aptiv forms to guide firms through regulatory path

The path toward securing regulatory approval for a device is becoming more and more tedious. In interviews with Medical Device Daily, many med-tech firms have spoken about how increasingly difficult and complex the process has been in the last two years. One company is hoping to give a helping hand to med-tech companies who need help in putting together a plan so that they can meet regulatory approval. (Medical Device Daily) Read More

Washington roundup: ReGen docs say firm expressed 'disdain' for FDA review process

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Report from Europe: STAAR gets two regulatory approvals for eye products

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Deals roundup: Hologic acquires Chinese distributor TCT for $135M

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Financings roundup: Sapiens raises €13 million for deep brain technology

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MDD's food for med-tech thought

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Court Report: Stockholders aim to block Stryker, Orthovita merger

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Agreements/contracts: Bovie, Medical Illumination work on lighting product

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HIT roundup: GE's patient management system installed at SLEH

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Product Briefs

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Patents roundup: DR Systems' PACS technology patent re-examined, allowed

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People in the News

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MDD's Ortho Extra

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