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BioWorld - Sunday, January 18, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

June 3, 2019

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Resolution's liquid biopsy assay for detecting HRD mutations gains breakthrough device designation

The U.S. FDA granted Resolution Bioscience Inc. breakthrough device designation for its cell-free DNA (cfDNA) assay, currently under development as a qualitative, in vitro companion diagnostic (CDx) to detect homologous recombination deficiency (HRD) mutations and gene deletions. Read More

Vesper raises $37M to back pivotal trial, PMA submission for deep venous stent

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Payer coverage cited as hurdle in HHS task force pain management report

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Take2 gets rights from Grail for NPC early detection technology

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Magnetic micro-robots allow targeted stem cell therapy

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Investors hoping for a slice of 3D laser technology that diagnoses, treats skin cancer

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TFF inhales another $8.2M to support thin film freezing tech

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Other news to note

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Daily M&A

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Regulatory front

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BioWorld MedTech stock report for public med-tech companies

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Product clinical data for May 31, 2019

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Product regulatory actions for May 31, 2019

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BioWorld MedTech's Neurology Extra

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