<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom">
<channel>
    <title><![CDATA[Kuvan (sapropterin dihydrochloride) - BioMarin International Limited]]></title>
    <ttl>1440</ttl>
    <copyright>Copyright: (C) European Commission</copyright>
    <language>en-gb</language>
    <atom:link href="http://ec.europa.eu/health/documents/community-register/html/rss/h481.rss" rel="self" type="application/rss+xml" />
    <lastBuildDate>Mon, 17 Jul 2017 12:07:00 +0000</lastBuildDate>
    <link>http://ec.europa.eu/health/documents/community-register/html/h481.htm</link>
    <description><![CDATA[Kuvan (Active substance: sapropterin dihydrochloride) - EU number: EU/1/08/481 - Marketing authorisation holder: BioMarin International Limited]]>
    </description>
    <image>
        <title><![CDATA[Kuvan (sapropterin dihydrochloride) - BioMarin International Limited]]></title>
        <url>http://ec.europa.eu/health/documents/community-register/images/logo_en.gif</url>
        <link>http://ec.europa.eu/health/documents/community-register/html/h481.htm</link>
        <width>144</width>
        <height>100</height>
    </image>
    <item>
        <title>Centralised - Variation - Commission Decision (2017)5083 of Mon, 17 Jul 2017</title>
        <category>New documents</category>
        <guid isPermaLink="true">http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc138199</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc138199</link>
        <description><![CDATA[Centralised - Variation) - Commission Decision (2017)5083 of Mon, 17 Jul 2017 - European Medicines Agency (EMA) procedure number: EMEA/H/C/943/X/47]]></description>
        <pubDate>Mon, 17 Jul 2017 12:07:00 +0000</pubDate>
    </item>
    <item>
        <title>Centralised - Variation - No Commission Decision</title>
        <category>No new document</category>
        <guid isPermaLink="true">http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc138417</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc138417</link>
        <description><![CDATA[Centralised - Variation) - No Commission Decision - European Medicines Agency (EMA) procedure number: EMEA/H/C/943/II/48/G]]></description>
        <pubDate>Thu, 22 Jun 2017 12:06:00 +0000</pubDate>
    </item>
    <item>
        <title>Centralised - Variation - No Commission Decision</title>
        <category>No new document</category>
        <guid isPermaLink="true">http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc137601</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc137601</link>
        <description><![CDATA[Centralised - Variation) - No Commission Decision - European Medicines Agency (EMA) procedure number: EMEA/H/C/943/II/46]]></description>
        <pubDate>Thu, 23 Mar 2017 12:03:00 +0000</pubDate>
    </item>
    <item>
        <title>Centralised - Yearly update - Commission Decision (2017)167 of Fri, 13 Jan 2017</title>
        <category>New documents</category>
        <guid isPermaLink="true">http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc136829</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc136829</link>
        <description><![CDATA[Centralised - Yearly update) - Commission Decision (2017)167 of Fri, 13 Jan 2017]]></description>
        <pubDate>Fri, 13 Jan 2017 12:01:00 +0000</pubDate>
    </item>
    <item>
        <title>Centralised - Variation - No Commission Decision</title>
        <category>No new document</category>
        <guid isPermaLink="true">http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc134140</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h481.htm#proc134140</link>
        <description><![CDATA[Centralised - Variation) - No Commission Decision - European Medicines Agency (EMA) procedure number: EMEA/H/C/943/IA/41]]></description>
        <pubDate>Wed, 27 Jan 2016 12:01:00 +0000</pubDate>
    </item>
    </channel>
</rss>
