Medical Device Manufacturer MRPC Bolsters Stringent Quality Program by Obtaining FDA 21 CFR 820 Compliance
MRPC, a leading single-source provider of medical device components and assemblies, has broadened the scope of its ISO 13485 certification to include the requirements of 21 CFR 820, the Food and Drug Administration s quality system regulations for medical devices sold in the U.S. (PRWeb December 15, 2010) Read the full story at http://www.prweb.com/releases/2010/12/prweb4902284 ...

FDA: Tainted Products Marketed As Dietary Supplements Potentially Dangerous
In a letter sent yesterday to dietary supplement manufacturers, the U.S. Food and Drug Administration expressed concern about undeclared or deceptively labeled ingredients in products marketed as dietary supplements. These substances include the active ingredients in FDA-approved drugs or their analogs (closely-related drugs), or other compounds, such as novel synthetic steroids, that do not ...