<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom">
<channel>
    <title><![CDATA[IDELVION (albutrepenonacog alfa) - CSL Behring GmbH]]></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/h1095.rss" rel="self" type="application/rss+xml" />
    <lastBuildDate>Fri, 21 Apr 2017 12:04:00 +0000</lastBuildDate>
    <link>http://ec.europa.eu/health/documents/community-register/html/h1095.htm</link>
    <description><![CDATA[IDELVION (Active substance: albutrepenonacog alfa) - EU number: EU/1/16/1095 - Marketing authorisation holder: CSL Behring GmbH]]>
    </description>
    <image>
        <title><![CDATA[IDELVION (albutrepenonacog alfa) - CSL Behring GmbH]]></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/h1095.htm</link>
        <width>144</width>
        <height>100</height>
    </image>
    <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/h1095.htm#proc137875</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h1095.htm#proc137875</link>
        <description><![CDATA[Centralised - Variation) - No Commission Decision - European Medicines Agency (EMA) procedure number: EMEA/H/C/003955/II/05]]></description>
        <pubDate>Fri, 21 Apr 2017 12:04:00 +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/h1095.htm#proc137671</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h1095.htm#proc137671</link>
        <description><![CDATA[Centralised - Variation) - No Commission Decision - European Medicines Agency (EMA) procedure number: EMEA/H/C/003955/IB/0006]]></description>
        <pubDate>Wed, 29 Mar 2017 12:03:00 +0000</pubDate>
    </item>
    <item>
        <title>Centralised - Notification - No Commission Decision</title>
        <category>No new document</category>
        <guid isPermaLink="true">http://ec.europa.eu/health/documents/community-register/html/h1095.htm#proc136231</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h1095.htm#proc136231</link>
        <description><![CDATA[Centralised - Notification) - No Commission Decision - European Medicines Agency (EMA) procedure number: EMEA/H/C/3955/N/0002]]></description>
        <pubDate>Wed, 28 Sep 2016 12:09:00 +0000</pubDate>
    </item>
    <item>
        <title>Centralised - Authorisation - Commission Decision (2016)2943 of Fri, 13 May 2016</title>
        <category>New documents</category>
        <guid isPermaLink="true">http://ec.europa.eu/health/documents/community-register/html/h1095.htm#proc134503</guid>
        <link>http://ec.europa.eu/health/documents/community-register/html/h1095.htm#proc134503</link>
        <description><![CDATA[Centralised - Authorisation) - Commission Decision (2016)2943 of Fri, 13 May 2016 - European Medicines Agency (EMA) procedure number: EMEA/H/C/3955]]></description>
        <pubDate>Fri, 13 May 2016 12:05:00 +0000</pubDate>
    </item>
    </channel>
</rss>
