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BioWorld - Sunday, March 1, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

April 2, 2019

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FDA permits Angiodynamics to initiate study with Nanoknife in pancreatic cancer

Angiodynamics Inc., of Latham, N.Y., said the U.S. FDA approved the company's investigational device exemption (IDE) application for its DIRECT study with Nanoknife. The study will evaluate the system in the treatment of stage III pancreatic cancer. Read More

Regulatory attorney says cybersecurity moves too quickly for effective rulemaking

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Cambridge Innovation Capital adds $197M to grow portfolio firms, support new startups

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Australian researchers develop organ-on-a-chip vascular model to reduce side effects of radiotherapy

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Court considers how much deference agencies like FDA should get in legal challenges

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Appointments and advancements

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Financings

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Regulatory front

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Product briefs

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Other news to note

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BioWorld MedTech's Cardiology Extra

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