Researchers have discovered a new way to detect per- and polyfluoroalkyl substances (PFAS) in water. This marks an important step forward in creating testing devices that are simpler, more ...

(NEXSTAR) – Over 141,000 bottles of cholesterol medication have been recalled due to “failed dissolution specifications,” suggesting that the drugs did not pass a solubility test, or failed to ...

GameSpot may get a commission from retail offers. The 1.0 version of Hades 2 is here, along with an assortment of questions and vague pointers about how to actually finish the story. Whether you're ...

At the heart of the case against the man accused of the Gilgo Beach killings is DNA evidence — but the novel way that evidence was tested may now determine whether prosecutors can use it against their ...

BILLERICA, Mass.--(BUSINESS WIRE)--Pion Inc., a leading provider of innovative analytical solutions for drug development, today announced the launch of its latest product, DissoSpec™ QC Dissolution ...

In the rapidly evolving 2025 consumer packaged goods (CPG) landscape, where market pressures demand faster, smarter decision making, breakthrough innovations don’t happen in isolation. They succeed in ...

The U.S. Food and Drug Administration said on Thursday that it will be phasing out the animal testing requirement for monoclonal antibody therapies and other drugs, replacing it with more ethical ...

April 10 (UPI) --The U.S. Food and Drug Administration is replacing animal testing with human-relevant methods, including artificial intelligence, when developing monoclonal antibody therapies and ...

The Confederation of European Paper Industries (CEPI), Brussels, has published an update to its European recyclability laboratory test method document, intended to help the paper and board industry ...

Laboratory-based design verification testing (DVT) of combination products and medical devices must be performed to demonstrate that the device meets the performance requirements that were set in the ...