The FDA has flagged three third-party labs that submitted device testing data that may have falsified, invalid or copied from ...
Morning Overview on MSN
The FDA cleared the first blood test to help diagnose Alzheimer’s in a doctor’s office
Adults showing signs of memory loss and cognitive decline can now be screened for Alzheimer’s disease with a simple blood ...
Visby Medical’s over the counter (OTC) combination PCR test for Covid-19 and influenza A/B detection has secured US Food and ...
SkylineDX’s test stratifies cutaneous melanoma patients into metastatic risk categories to inform treatment decisions.
The FDA could approve the first blood test that can detect multiple cancers, around the end of the year, setting the stage ...
As FDA continues to work under Operation Stork Speed and Closer to Zero, the question remains whether the data will translate into binding standards – or remain a category snapshot. FDA released ...
FDA admonishes Chinese device testing lab for falsified studies, copied data The US Food and Drug Administration (FDA) on Monday published a letter to Chinese medical device testing firm Mid-Link ...
The US Food and Drug Administration (FDA) roadmap to reduce animal testing as a requirement for drug development has already made an impact after its first year, but the initiative faces future ...
On November 28, 2025, the U.S. Food and Drug Administration (FDA) withdrew its 2024 proposed rule entitled “Testing Methods for Detecting and Identifying Asbestos in Talc-Containing Cosmetic Products.
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