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	<title>QA/RA Updates for Medical Device Professionals &#187; UK</title>
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	<description>International Quality and Regulatory Compliance Updates for the Medical Device Industry</description>
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		<title>MHRA publishes updated guidance document for clinicals conducted in UK</title>
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		<pubDate>Wed, 12 Aug 2009 19:43:15 +0000</pubDate>
		<dc:creator>Chris Schorre, Emergo Group</dc:creator>
				<category><![CDATA[Regulatory Affairs]]></category>
		<category><![CDATA[clinical]]></category>
		<category><![CDATA[MHRA]]></category>
		<category><![CDATA[UK]]></category>

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		<description><![CDATA[In July, the MHRA issued an updated guidance document on clinical investigations to be carried out in the UK. It’s an update on previously available guidance that takes into account the impact of 2007/47/EC, the revision to the directives which takes effect in March 2010. One of the major updates in this document is the confirmation [...]]]></description>
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