FDA Issues Warnings to Marketers of Unapproved “Chelation” Products

On October 14, 2010, FDA warned eight companies that market over-the-counter chelation products that these are unapproved drugs and devices and that it is a violation of federal law to make false claims about the products.

Source: http://www.fda.gov/NewsEvents/PublicHealthFocus/ucm228685.htm

supplier Docetaxel Docetaxel clinical trial Docetaxel structure

Leave a Reply

Your email address will not be published. Required fields are marked *

*

You may use these HTML tags and attributes: <a href="" title=""> <abbr title=""> <acronym title=""> <b> <blockquote cite=""> <cite> <code> <del datetime=""> <em> <i> <q cite=""> <strike> <strong>