The US Food and Drug Administration (FDA) says it is discontinuing one of its audit-sharing pilots ahead of the launch of a "fully operational" Medical Device Single Audit Program (MDSAP) in 2017. FDA ...
The US Food and Drug Administration (FDA) has issued warning letters to a device maker and several drug makers for failing to ...
Why continuous audit readiness helps MedTech organizations move faster—without sacrificing confidence or control.
The U.S. Food and Drug Administration (FDA) recently announced the results of its pilot program evaluating whether several third-party food safety standards align with the food safety requirements in ...
This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. The U.S. Food and Drug Administration took ...
Pharmaceutical company AvKare has issued a voluntary recall on several of its over-the-counter products for dry and irritated eyes, citing regulatory "deviations" identified during an audit by the ...
The U.S. Food and Drug Administration took more than 15 months to act on a whistleblower complaint it received about conditions at an Abbott Nutrition factory that was at the center of a nationwide ...
FILE - A sign at an Abbott Laboratories campus facility is displayed, April 28, 2016, in Lake Forest, Ill. A report released on Thursday, June 13, 2024, says the U.S. Food and Drug Administration took ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results