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BioWorld - Wednesday, December 31, 2025
Home » Topics » Regulatory, BioWorld MedTech

Regulatory, BioWorld MedTech
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FDA authorizes Pear Therapeutics' prescription digital insomnia therapy

March 27, 2020
By Annette Boyle
Pear Therapeutics Inc. obtained FDA approval for Somryst, the first prescription digital therapeutic for chronic insomnia. The app provides structured cognitive behavior therapy (CBT) with clinical dashboards for physicians. While CBT is the recommended first-line therapy for insomnia, the U.S. has only 500 therapists certified to provide CBT for insomnia (CBTi) for the estimated 30 million Americans who suffer from chronic difficulty going to and staying asleep.
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European Union flag

EU pulling the plug on MDR implementation

March 27, 2020
By Nuala Moran
LONDON – The European Commission (EU) is pulling the plug on implementation of the Medical Devices Directive (MDR) on May 26, to free up resources and expertise as countries across Europe struggle to deal with the COVID-19 crisis.
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COVID-19: With cases growing In Latin America, the race to keep patients breathing is on

March 27, 2020
By Sergio Held
BOGOTA, Colombia – The global shortage of ventilators caused by COVID-19 is not news to the Latin American region, an area already preparing for the tsunami of patients that could flood hospitals as it has done elsewhere. The region is trying to learn from the mistakes made by European countries before it is too late.
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Regulatory front for March 27, 2020

March 27, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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FDA greenlights novel ablation system for heavy menstrual bleeding

March 27, 2020
By Meg Bryant
Aegea Medical Inc., of Menlo Park, Calif., has received U.S. FDA approval for its next-generation Mara water vapor ablation system, the only endometrial ablation treatment that uses vapor to treat heavy menstrual bleeding. The first commercial procedure was performed by Kirk Brody, an obstetrician-gynecologist in Chattanooga, Tenn.
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Regulatory front for March 26, 2020

March 26, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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In the clinic for March 26, 2020

March 26, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Castle Biosciences.
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Hand holding FDA blocks

Test developers frustrated by FDA’s resistance to at-home testing

March 25, 2020
By Mark McCarty
The surge of interest in testing for the COVID-19 pathogen has led to some innovative tests and test strategies, including at-home tests. However, the FDA has indicated that it is wary of both at-home testing and specimen collection in other than supervised settings, a policy that is meeting with criticism from some quarters, but not all.
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FDA OKs Align Technology’s Itero Element 5D dental scanner

March 25, 2020
By Meg Bryant
San Jose, Calif.-based Align Technology Inc. has won the FDA’s nod for its Itero Element 5D imaging system. The company said the Itero Element 5D is the first intraoral scanner with near-infrared imaging (NIRI) technology that visualizes the internal structure of the tooth in real time. The FDA cleared the device for the detection of interproximal caries lesions above the gingiva and for monitoring the progress of such lesions.
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Regulatory front for March 25, 2020

March 25, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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