Judge Orders Health Agencies to Restore Web Pages That Trump Team Removed
In a two-page ruling, U.S. District Judge John Bates ordered HHS, the FDA and the CDC to restore the pages and datasets identified in DFA's complaint. Some of the pages that were taken down were: ...
GlobalData on MSN2d
ImpediMed secures $15m in funding to support SOZO platform
ImpediMed has received $15m in funding for five years from SWK Holdings, which is set to enhance its ability to grow and ...
Hosted on MSN5d
FDA grants breakthrough designation for Acrivon’s endometrial cancer assay
The US Food and Drug Administration (FDA) has granted breakthrough device designation for Acrivon Therapeutics’ ACR-368 ...
U.S. News & World Report13d
US FDA Identifies Cybersecurity Risks in Certain Patient Monitors
(Reuters) - The U.S. Food and Drug Administration (FDA) said on Thursday it had identified three cybersecurity risks associated with certain patient monitors from Contec and Epsimed and urged ...
Morningstar28d
Radical Catheter Technologies’ 8F Neurovascular Catheter Receives US FDA 510(k) Clearance, Second for the Best-in-Class Ribbon Technology Platform
Radical Catheter Technologies has received two US FDA 501(k) clearances for the 7F and 8F applications of its novel platform. The 7F Radical™ Catheter has neurovascular clearance for both ...
Al Jazeera English27d
What is Red Dye 3 and why has the US FDA banned it in food and drinks?
In November 2024, nearly two dozen Congress members sent a letter to the FDA officials demanding a ban on the dye. But the decision taken by the organisation also comes amid US President-elect ...
Morningstar7d
FDA Accepts Integral Molecular's Membrane Proteome Array™ Qualification Plan, Advancing the Platform for Approval as a Drug Development Tool
Integral Molecular's MPA is the industry-leading technology for antibody specificity testing and is the only specificity platform under FDA consideration as a DDT. Learn more about the Membrane ...
Yahoo Finance28d
Radical Catheter Technologies’ 8F Neurovascular Catheter Receives US FDA 510(k) Clearance, Second for the Best-in-Class Ribbon Technology Platform
Built on the same patented platform as Radical’s 7F catheter, the first FDA-cleared product from the ... expand our platform further and propel us into a full commercial launch.” ...