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	<title>Drug Development Consultant and Regulatory Consultant &#187; evaluation</title>
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		<title>Drug Regulators, EMEA, Release Overview of Comments Received on Draft Guidance on Clinical Evaluation of Diagnostic Agents</title>
		<link>http://www.damienbove.com/2010/02/05/drug-regulators-emea-release-overview-of-comments-received-on-draft-guidance-on-clinical-evaluation-of-diagnostic-agents/</link>
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		<pubDate>Fri, 05 Feb 2010 15:48:45 +0000</pubDate>
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				<category><![CDATA[clinical]]></category>
		<category><![CDATA[Diagnostic Agents]]></category>
		<category><![CDATA[evaluation]]></category>

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			<content:encoded><![CDATA[<h1>Drug Regulators, EMEA, Release Overview of Comments Received on Draft Guidance on Clinical Evaluation of Diagnostic Agents.</h1>
<p>Full Text <a title="EMEA Guidance" href="http://www.ema.europa.eu/pdfs/human/ewp/18247009en.pdf " target="_blank">here</a></p>
<p>Comments contributed by:</p>
<p>1 Industry Task Force and AIPES<br />
2 EORTC<br />
3 GE Healthcare LTD<br />
4 International Society for Clinical Biostatistics (ISCB)<br />
5 MSD<br />
6 Novartis Pharma<br />
7 Jorgen Hilden (Dept of Biostatistics, University of Copenhagen)<br />
8 Anabel Cortes-Blanco</p>
<p>Damien Bové is THE Drug Development and Regulatory Consultant (pharmaceutical or biotechnology), I work with my clients to define a drug development target, define a drug development strategy, define a regulatory strategy or define a commercial strategy. Our clients are generally raising funds or looking to license out their technology and we help them achieve it. If you want to know more don’t hesitate to get in touch.</p>
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