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BioWorld - Tuesday, May 13, 2025
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Home » Topics » BioWorld MedTech, Regulatory

BioWorld MedTech, Regulatory
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Product regulatory actions for Sept. 17, 2019

Sep. 18, 2019

Dreamed wins U.S. and EU approval for AI-based insulin recommendation technology

Sep. 18, 2019
By David Ho
HONG KONG – Dreamed Diabetes Ltd., of Petah Tikva, Israel, has received both FDA clearance and the CE mark for an insulin dosing decision support software based on artificial intelligence (AI).
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Regulatory front

Sep. 17, 2019

Product regulatory actions for Sept. 16, 2019

Sep. 17, 2019

Gala Therapeutics gets breakthrough device designation for Rheox system

Sep. 17, 2019
By Liz Hollis
Chronic bronchitis affects more than 9 million people in the U.S., but current treatments fail to address the overproduction of mucus. Gala Therapeutics Inc., of Menlo Park, Calif., is looking to change that.
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Australia proposes revising device essential principles to align with international practices

Sep. 17, 2019
By Tamra Sami
PERTH, Australia – The Therapeutic Goods Administration (TGA) is seeking feedback on a proposal that to change Australia's medical device essential principles for safety and performance to more closely mirror the new EU Medical Device Regulation (EU MDR).
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FDA advisory committee suggests disclosure of cybersecurity risks should be only to patients

Sep. 17, 2019
By Mark McCarty

Product regulatory actions for Sept. 13, 2019

Sep. 16, 2019

Prescient Metabiomics granted breakthrough status for noninvasive colorectal cancer test

Sep. 16, 2019
By Annette Boyle
The FDA granted breakthrough device status to Prescient Metabiomics' Lifekit Prevent colorectal neoplasia test. Prescient Metabiomics is a subsidiary of Carlsbad, Calif.-based Prescient Medicine Holdings Inc.
Read More

ACC inks decision pathway for heart failure, apps to follow

Sep. 16, 2019
By Mark McCarty
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