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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

June 3, 2019

View Archived Issues

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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