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	<title>QA/RA Updates for Medical Device Professionals &#187; eLabeling</title>
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	<description>International Quality and Regulatory Compliance Updates for the Medical Device Industry</description>
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		<title>Taking advantage of elabeling for IVD companies</title>
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		<pubDate>Wed, 18 Feb 2009 14:12:36 +0000</pubDate>
		<dc:creator>Chris Schorre, Emergo Group</dc:creator>
				<category><![CDATA[Regulatory Affairs]]></category>
		<category><![CDATA[eLabeling]]></category>
		<category><![CDATA[IVD]]></category>

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		<description><![CDATA[In 2007 the European Commission released MEDDEV 2.14/3 REV 1 which opened the door for IVD companies with professional use products to place their Instructions for Use (IFU) online instead of placing multilingual paper inserts inside product packaging. That could be a huge cost savings to some IVD companies  but one key requirement makes it [...]]]></description>
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