RAPS

This Week at FDA: FDA names PreCheck participants, TAP open to all OHT devices, and more

Welcome to another installment of This Week at FDA, your weekly source for updates – big and small – on FDA, drug and medical device regulation, and what we’re reading from around the web. This week, ...
RAPS

Recon: FDA approves Vertex gene therapy for children with sickle cell disease; Judge blocks Colorado price cap on Amgen’s Enbrel

Regulatory Recon is our regular intelligence briefing for the regulatory affairs space, bringing you the top regulatory, biopharma and medtech news stories from around the globe. Regulatory Recon is ...
Yahoo

FDA updates Hologic BioZorb recall, citing 252 injuries

Add Yahoo as a preferred source to see more of our stories on Google. The Food and Drug Administration has reported 252 injuries were associated with Hologic's BioZorb radiographic markers implanted ...
medtechdive

FDA updates Hologic BioZorb recall, citing 252 injuries

Following the recall, Hologic received a warning letter from the FDA in December 2025. The agency found the company failed to meet design requirements for the markers and raised concerns about ...
Nature

Paxillin and focal adhesion signalling

The adhesion of cells to the surrounding extracellular matrix and their stimulation by soluble growth factors provide the environmental cues necessary to control a cell's decision to survive, ...
medtechdive

ECRI CEO: FDA, industry must revisit COVID-19 medical device EUAs as shortages ebb

As the pandemic intensified in the U.S., FDA granted emergency use authorizations for a slew of medical devices to fill shortages of crucial medical supplies when hospitals began filling up with COVID ...