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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

May 17, 2019

View Archived Issues

Aidoc scores win at FDA with PE solution

Tel Aviv, Israel-based Aidoc Ltd. has received the green light from the U.S. FDA for its pulmonary embolism (PE) product in its suite of artificial intelligence (AI)-based workflow orchestration solutions. Its latest offering aims to help radiologists flag and triage PE cases in chest CTs. The company is looking to cut the time from scan to diagnosis, which could mean for some patients a result in less than five minutes vs. hours – thereby speeding up treatment and improving prognosis. Read More

Pivotal trial shows T2 sepsis test is faster, more accurate than standard blood culture

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Digital technology now a health care mainstay

TEL AVIV, Israel – The use of digital technologies in medical technology is rapidly moving well beyond efforts to organize data or communicate long distance. Multiple companies are now working to use digital technologies to address medical conditions and improve therapeutic outcomes. While some of these companies are technology companies that have taken something of a back door into health care through consumer products (like the Iwatch or Fitbit that can be used to track metabolic activity or by providing technology platforms like Amazon or Microsoft), other entrants are health care companies first that use digital technology to meet health care goals. Read More

Korea to collaborate with Italy, Japan on cancer biomarker

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Phage therapy treats drug-resistant mycobacterial infection

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Other news to note

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Appointments and advancements

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Regulatory front

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Financings

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Product clinical data for May 16, 2019

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Product regulatory actions for May 16, 2019

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BioWorld MedTech's Diagnostics Extra

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