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Crescendo Touts Rheumatoid Arthritis Dx Data Haul At ACR2016

 
• By Reed Miller

Crescendo Bioscience, a wholly-owned subsidiary of Myriad Genetics, is talking-up the results of four different clinical trials of its Vectra DA multi-analyte blood test for rheumatoid arthritis that were presented at this year's American College of Rheumatology meeting in Washington, DC.

Crescendo Bioscience Inc. has received a boost from new clinical data that supports the use of its Vectra DA multi-analyte blood test to predict the progression of rheumatoid arthritis (RA) and suggest it can help physicians make better treatment choices for RA patients.

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LSX Roundup: Startups Elypta, QuantiLight And Plexaa Debut New Tech

 
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Back-to-back meetings at LSX? No time to attend the innovator showcase? Here is what you might have missed from medtech innovators at the LSX World Congress Europe on 29 April.

‘The FDA Will Be Looking For Avenues To Regulate Laboratory Developed Tests’

 
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The FDA's final LDT ruling was struck down in federal court last month. For now, diagnostic companies can commercialize under CLIA regulations or apply for FDA approval. McDermott and Tribun Health have shared insights on the risks, pros and cons of both regulatory routes.

First Liver Cancer Surveillance Test In Five Years Receives FDA Breakthrough Status

 
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OneCell Diagnostics – Now 1Cell.Ai - Launches Multi-Modal Cancer Diagnostic Panel OncoIncytes

 
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OneCell Diagnostics, the Mumbai-based startup backed with $16m in series A funding, is rebranding to 1Cell.Ai to represent the firm's focus on combining deep science with AI-powered capabilities.

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‘The FDA Will Be Looking For Avenues To Regulate Laboratory Developed Tests’

 
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AdvaMed Unveils Its First ‘AI Roadmap’ To Help Lawmakers Navigate Regulating The Technology Through Rocky Times

 
• By Brian Bossetta

Members of AdvaMed’s digital health tech board of directors discussed the organization’s efforts to aid the Trump administration and Congress in answering AI policy questions, especially as companies deal with mounting regulatory uncertainty.

First Liver Cancer Surveillance Test In Five Years Receives FDA Breakthrough Status

 
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