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	<title>QA/RA Updates for Medical Device Professionals &#187; 93/42/EEC</title>
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	<description>International Quality and Regulatory Compliance Updates for the Medical Device Industry</description>
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		<title>European Commission issues important guidance document on 2007/47/EC</title>
		<link>http://www.qara.info/regulatory/guidance-document-2007-47-ec/</link>
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		<pubDate>Thu, 11 Jun 2009 16:37:03 +0000</pubDate>
		<dc:creator>Chris Schorre, Emergo Group</dc:creator>
				<category><![CDATA[Regulatory Affairs]]></category>
		<category><![CDATA[2007/47/EC]]></category>
		<category><![CDATA[93/42/EEC]]></category>

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		<description><![CDATA[The EU has just released an important guidance document that should be read by every company selling medical devices in Europe. It provides guidance on an amendment to the original Medical Devices and Active Implantable Medical Devices Directives. Probably the most important part of the 2007/47/EC guidance for medical device companies is that the amended [...]]]></description>
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