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BioWorld - Saturday, December 20, 2025
Home » Topics » Regulatory

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FDA approves Taltz for pediatric patients with plaque psoriasis

March 31, 2020
Coronavirus microscopic model

Ottawa issues order accelerating delivery of U.S. made COVID-19 test kits

March 30, 2020
By David Godkin
TORONTO – The Government of Canada is fast tracking importation of two U.S. manufactured test kits for COVID-19, issuing an interim order for sale of the Cobas SARS-CoV-2 diagnostic test kit developed by Pleasanton, Calif.-based Roche Molecular Systems Inc. and Waltham, Mass.-based Thermo Fisher Scientific Inc.’s Taqpath COVID-19 Combo Kit.
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Regulatory front for March 30, 2020

March 30, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Medtronic.
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FDA urges further steps to avoid drug shortages

March 30, 2020
By Mari Serebrov
To mitigate COVID-19-related drug shortages, the FDA issued new guidance reminding drug and biologic manufacturers of their legal obligations to notify the agency, in advance, of interruptions or the permanent discontinuance in the manufacturing of certain drugs. It also makes some new recommendations in light of the current emergency.
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Regulatory front for March 30, 2020

March 30, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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FDA approves Imfinzi as first-line treatment for extensive-stage SCLC

March 30, 2020
3-27-Pear-Somryst.png

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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3-27-OxyGEN-LatAm.png

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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