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BioWorld - Sunday, December 21, 2025
Home » Topics » Regulatory, BioWorld MedTech

Regulatory, BioWorld MedTech
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DNA-based Spartan Cube to test for COVID-19 in Canada

April 23, 2020
By David Godkin
TORONTO – A portable DNA-based test kit developed by Ottawa-based Spartan Bioscience Inc. has received Health Canada approval for COVID-19 testing – this at a time when hospitals are under enormous pressure to meet increased testing demand.
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Regulatory front for April 23, 2020

April 23, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: KPMD.
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Regulatory action for April 23, 2020

April 23, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Agilent, Baxter, Biocomposites, Cagent Vascular, Mevion.
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Map of Latin America, South America

Med-tech companies in Argentina and Brazil ramp up ventilator production

April 22, 2020
By Sergio Held
BOGOTA, Colombia – Med-tech companies across Latin America that have traditionally focused on domestic and regional markets are in a race against time to supply ventilators to deal with worsening COVID-19 outbreaks.
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Regulatory front for April 22, 2020

April 22, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Predictive Technology Group, SC Worx, Spectrum DNA.
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Regulatory action for April 22, 2020

April 22, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Life Spine, Mobidiag, Seegene.
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U.S. FDA headquarters

FDA gives Labcorp the nod for Pixel home collection swab, but access limited for now

April 21, 2020
By Mark McCarty
The U.S. FDA reported that it has expanded the emergency use authorization for the Labcorp polymerase chain reaction (PCR) test for SARS-CoV-2 to include the company’s Pixel self-collection kit, a development that may presage a wider testing paradigm that is needed to restore the U.S. economy to normalcy.
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Incyte wins FDA approval for first targeted cholangiocarcinoma treatment

April 21, 2020
By Michael Fitzhugh
With a coronavirus task force briefing unfolding at the White House late on April 17, an FDA eager to show its ongoing commitment to tackling other disease amid the pandemic, granted accelerated approval to Incyte Corp.'s Pemazyre (pemigatinib), the first treatment approved for adults with certain types of previously treated, advanced cholangiocarcinoma.
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Regulatory front for April 21, 2020

April 21, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
Read More

Regulatory action for April 21, 2020

April 21, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Brainlab, Inspire Medical Systems, Labcorp, Roche.
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