Topic: Food and Drug Administration
(Reuters) - Diagnostics products maker Neoprobe Corp said U.S. health regulators have indicated that data from a late-stage trial of its radioactive tracing agent would support filing for marketing approval. The company recently met the U.S. Food and Drug Administration to review the late-stage trial results of its experimental radioactive tracing agent, Lymphoseek, which seeks to determine the spread ...
Watson Pharmaceuticals Inc. said the Food and Drug Administration approved a six-month dose of the prostate cancer drug Trelstar, which already was available in one- and three-month doses. Trelstar is developed by Debiopharm Group of Switzerland and marketed by Watson. Watson plans to launch the six-month dose in ...
The use of supplements is a normal part of people?s personal health care, to the point that one rarely needs a prescription to buy any. Supplements can also provide the right amounts of certain nutrients that are hard to get regularly, or are present in only very tiny amounts in our food.
A bit of state regulation of dietary ...
The Food and Drug Administration is warning doctors and patients about counterfeit surgical mesh being illegally marketed under the C.R. Bard brand name. The FDA has identified thirteen lots of Bard Flat Mesh that were not actually made by the company. The counterfeit products come ...
