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	<title>Drug Development Consultant &#38; Regulatory Consultant &#187; Business Requirements of ICH</title>
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		<title>Drug Regulators Publish, ICH M2, Business Requirements Guidance</title>
		<link>http://www.damienbove.com/2009/12/25/drug-regulators-publish-ich-m2-business-requirements-guidance/</link>
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		<pubDate>Fri, 25 Dec 2009 10:00:39 +0000</pubDate>
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				<category><![CDATA[business]]></category>
		<category><![CDATA[regulatory]]></category>
		<category><![CDATA[Business Requirements of ICH]]></category>
		<category><![CDATA[ICH]]></category>
		<category><![CDATA[ICH M2]]></category>

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		<description><![CDATA[ICH M2 has initiated the development of the Next Major Version of the eCTD (eCTD NMV) to improve robustness, flexibility and long term stability of the message. <a href="http://www.damienbove.com/2009/12/25/drug-regulators-publish-ich-m2-business-requirements-guidance/">Continue reading <span class="meta-nav">&#8594;</span></a>]]></description>
			<content:encoded><![CDATA[<h1>Drug Regulators Publish, ICH M2, Business Requirements Guidance.</h1>
<p>Full Text <a title="EMEA Guidance" href="http://www.emea.europa.eu/pdfs/human/ich/79247609enfin.pdf " target="_blank">Here</a></p>
<p>ICH M2 has initiated the development of the Next Major Version of the eCTD (eCTD NMV) to improve robustness, flexibility and long term stability of the message. In accordance with the decision by the ICH Steering Committee that technical specifications should no longer be developed solely within ICH, but should be created in collaboration with Standards Development Organisations (SDOs), the eCTD NMV will be developed jointly with the HL7 RPS project. M2 has developed the following list of requirements as input into the HL7 RPS Project.<br />
Damien Bové works as a drug development consultant (pharmaceutical or biotechnology) and regulatory consultant, we work with our 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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<div id="_mcePaste" style="overflow: hidden; position: absolute; left: -10000px; top: 0px; width: 1px; height: 1px;">This guideline ap</div>
<div id="_mcePaste" style="overflow: hidden; position: absolute; left: -10000px; top: 0px; width: 1px; height: 1px;">recombinant vaccines for the prevention and treatment of infectious disease, and provides guidance on quality, non-clinical and clinical aspects.</div>
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<dt class="wp-caption-dt"><a href="http://www.damienbove.com/?page_id=183"><img class="size-full wp-image-191" style="padding: 0px; margin: 0px; border: 0px none initial;" title="Free Strategy Consultation - Biotech Pharma Regualtory" src="http://www.damienbove.com/wordpress/wp-content/uploads/2009/04/ida_consultants_freestrategyconsultation_515x64.jpg" alt="ida consultants freestrategyconsultation 515x64 Drug Regulators Publish, ICH M2, Business Requirements Guidance" width="515" height="64" /></a></dt>
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