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    <title>Marc Ullman FYI Blog</title>
    <description>&lt;img src="http://www.npicenter.com/images/MarcUllman.gif" border="0" align="left"&gt;Mr. Ullman speaks frequently on various regulatory matters at various events, including Virgo Publications' Natural Products Industry Supply Side West Trade Shows and the National Nutritional Foods Association's annual MarketPlace Convention.  He also manages the FYI Newsletter highlighting legal and regulatory issues concerning the Natural Product Industry.  &lt;br&gt;&lt;br&gt;Marc is a partner in New York City based Ullman, Shapiro &amp; Ullman, &lt;a href="http://www.usulaw.com"&gt;www.usulaw.com&lt;/a&gt;. You can contact him at Marc[at]usulaw.com&lt;br&gt;&lt;br&gt;&lt;i&gt;Please note that blog is not intended to provide or serve as legal advice of any kind, and that the reader should not rely on it for such advice.&lt;/i&gt;  </description>
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    <pubDate>Fri, 16 May 2008 17:34:25 GMT</pubDate>
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      <title>IF YOU WANT TO MARKET A NEW INGREDIENT OR TRANSITION FROM SUPPLEMENT TO FOOD, THERE’S SOMETHING YOU NEED TO KNOW</title>
      <description>On September 27, 2007 President Bush signed into law the Food and Drug Administration Amendments Act of 2007 (FDAAA).  Ostensibly designed to strengthen FDA’s authority over a variety of regulated areas such as food safety and post-market surveillance of drug products, the law contains a provision that has the potential to greatly restrict the entry crossover of dietary supplement ingredients to food and the introduction of dietary supplement ingredients into the marketplace.</description>
      <link>http://www.npicommunity.com/Blogs/tabid/53/EntryID/103/Default.aspx</link>
      <author>marc@usulaw.com</author>
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      <pubDate>Thu, 28 Feb 2008 20:00:00 GMT</pubDate>
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