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BioWorld - Saturday, March 21, 2026
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BioWorld MedTech
Dec. 26, 2013
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Company looking to streamline its regulatory path by packaging products
PARIS – Imagine that every new software application needs to first pass a regulatory review.That's the business case faced by any vendor of post-processing software for medical imaging.
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FDA clears Philips' new spectral breast density measurement tool
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Washington Roundup: NICE urges coverage of PFO procedure; registry mandated
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Shinva Medical continues to raise its profile through acquisitions
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Agreements/Contracts: CombiMatrix, FedMed enter into diagnostic laboratory services pact
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Financings roundup: Medgenics founder establishes personal stock trading plan
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HIT roundup: Adoption of cloud-based solutions on the rise
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Med-tech news & Notes: Intuitive Cites Robotic-Assisted Surgery Study
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Product briefs:
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Keeping you up to date with recent developments in orthopedics:
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