Latest FDA Stories
Despite Strict FDA Approval Process, Product Launches Will Support Market Growth, According to Findings from Decision Resources Group BURLINGTON, Mass., Oct.
Validation of manufacturing process changes for the MGuard Prime EPS BOSTON, Oct.
SAN DIEGO, Oct. 29, 2014 /PRNewswire/ -- Aethlon Medical, Inc.
FREIBURG and HEIDELBERG, Germany, October 29, 2014 /PRNewswire/ -- Positive FDA feedback on the protocol for the US Phase III trial with LT-02,
Is the de novo process right for a particular medical device? To help manufacturers decide, FDAnews is pleased to present a 90-minute webinar on Nov.
MedicinesMexico.com is a Mexico pharmacy online that meets FDA guidelines and offers a number of brand name and generic blood pressure medicines.
On October 25, the FDA announced that two lots of INTRAVIA containers, by Baxter International, in the U.S. and Canada are recalled due to particulate matter.
TARRYTOWN, N.Y., Oct.
The FDA's enforcement plan makes it clear: Developing a successful CAPA program has never been more important. FDAnews and Compliance Media, Inc.
FDA has published a newlist of licensed biological products and interchangeable biosimilars, the “Purple Book”, which is being hyped as being the biological equivalent of the pharmaceutical
- The act of sweetening by admixture of some saccharine substance.