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BioWorld - Wednesday, May 14, 2025
Breaking News: US FDA clears Abbvie’s c-Met lung cancer ADC Breaking News: 100 days of uncertaintyBreaking News: 100 days of uncertainty
Home » Topics » BioWorld MedTech, Regulatory

BioWorld MedTech, Regulatory
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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

BARDA deal could provide T2 Biosystems up to $69M

Sep. 16, 2019
By Meg Bryant

Regulatory front

Sep. 16, 2019

FDA retains 'well-defined' restriction in special 510(k) final

Sep. 13, 2019
By Mark McCarty

Health of U.S. patent system in the eye of the beholder

Sep. 13, 2019
By Mari Serebrov
Depending on who's talking, the U.S. patent system may, or may not, be in dire need of reform. In a Senate Judiciary subcommittee hearing Wednesday on the bipartisan STRONGER Patents Act, Sen. Chris Coons (D-Del.) stressed the need to undo the precedent set by the Supreme Court's 13-year-old eBay decision that weakened injunctive relief in infringement cases and to resolve some of the unintended consequences of the 2011 America Invents Act (AIA).
Read More

Product regulatory actions for Sept. 12, 2019

Sep. 13, 2019

Product regulatory actions for Sept. 11, 2019

Sep. 12, 2019
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