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	<title>Medpoint &#187; Open Projects</title>
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	<link>http://www.medpoint.com</link>
	<description>Device, Pharmaceutical, Biotech</description>
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		<title>2009 Completed Projects</title>
		<link>http://www.medpoint.com/2008-completed-projects/</link>
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		<pubDate>Fri, 12 Feb 2010 21:17:46 +0000</pubDate>
		<dc:creator>PECULIAR</dc:creator>
				<category><![CDATA[Open Projects]]></category>

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		<description><![CDATA[Creator – Supplier Quality System &#8211; (USA) Acting Director Regulatory Affairs – (USA) DHF Project Lead – Major Device – (USA) Mock FDA Audit (3) – (USA) International internal audit – (Germany) Regulatory Strategist – (USA) Acting Quality Manager (3) – (USA) Validation Team Lead – (USA) MRB support – (USA) Engineering Protocols Reviewer (2) [...]]]></description>
			<content:encoded><![CDATA[<p>Creator – Supplier Quality System &#8211;  (USA)</p>
<p>Acting Director Regulatory Affairs – (USA)</p>
<p>DHF Project Lead – Major Device – (USA)</p>
<p>Mock FDA Audit (3) – (USA)</p>
<p>International internal audit – (Germany)</p>
<p>Regulatory Strategist – (USA)</p>
<p>Acting Quality Manager (3) – (USA)</p>
<p><a href="http://medpoint.timpecoraro.com/wp-content/uploads/2008/10/mission.gif" rel="shadowbox[post-289];player=img;"><img class="aligncenter size-full wp-image-291" title="mission" src="http://medpoint.timpecoraro.com/wp-content/uploads/2008/10/mission.gif" alt="" width="300" height="125" /></a>Validation Team Lead – (USA)</p>
<p>MRB support – (USA)</p>
<p>Engineering Protocols Reviewer (2) – (USA)</p>
<p>MDR Project Lead – (USA)</p>
<p>International FDA audit – (New Zealand)</p>
<p>Quality Engineer (7) – (USA)</p>
<p>Acting Global Head RA &#8211; IVD – (USA)</p>
<p>Creator Quality System – (USA)</p>
<p>Global Regulatory Strategist – (Japan)</p>
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