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BioWorld - Friday, July 10, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

March 11, 2019

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FDA grants the first breakthrough device designation for AI in cancer Dx

New York-based startup Paige.AI has gained the first disclosed breakthrough device designation from the U.S. FDA for the application of artificial intelligence (AI) in cancer diagnosis. Pathology is an obvious early place for AI in health care; it's imaging-heavy, and a segment where AI is already being integrated. In addition, there's a high degree of variability between pathologists in their assessments, while digital pathology slides are becoming more commonplace, and patient outcomes could be improved by more accurate, consistent pathology reports. Read More

Series A pumps $11M into Cerebral's epilepsy efforts; drug-device IND just ahead

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US, Canadian firms tackle opioid crisis with subdermal implant

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New Zealand's Volpara AI algorithms could have massive implications for breast cancer screenings

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Despite funding challenges, Indian health startups see promise in devices

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Industry blasts draft de novo rule over pre-grant inspection

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Appointments and advancements

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Regulatory front

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BioWorld MedTech stock report for public med-tech companies

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Financings

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Daily M&A

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Product briefs

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Other news to note

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BioWorld MedTech's Neurology Extra

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