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	<title>23 october &#8211; Eisner Safety Consultants</title>
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	<link>https://eisnersafety.com</link>
	<description>Regulatory &#38; Safety Experts for Global Medical Device Approvals</description>
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	<title>23 october &#8211; Eisner Safety Consultants</title>
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		<title>White Paper on Proposed New EU Medical Device Regulations</title>
		<link>https://eisnersafety.com/2012/10/25/white-paper-on-proposed-new-eu-medical-device-regulations/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=white-paper-on-proposed-new-eu-medical-device-regulations</link>
		
		<dc:creator><![CDATA[leoeisner]]></dc:creator>
		<pubDate>Thu, 25 Oct 2012 00:38:01 +0000</pubDate>
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		<category><![CDATA[23 october]]></category>
		<category><![CDATA[26 Sept]]></category>
		<category><![CDATA[26 Sept '12]]></category>
		<category><![CDATA[26 Sept 2012]]></category>
		<category><![CDATA[Active Implantable Medical Devices Directive]]></category>
		<category><![CDATA[AIMDD]]></category>
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		<category><![CDATA[MDD]]></category>
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		<category><![CDATA[Medical]]></category>
		<category><![CDATA[Medical Device]]></category>
		<category><![CDATA[Medical Device Directive]]></category>
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		<category><![CDATA[Medical Device Regulatory]]></category>
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		<category><![CDATA[Proposal]]></category>
		<category><![CDATA[Proposed New Medical Device Regulations for Europe]]></category>
		<category><![CDATA[White Paper on Proposed New Medical Device Regulations 2012]]></category>
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					<description><![CDATA[The Emergo Group issued a White Paper on 22 October 2012 in regard to the 26 September 2012 Proposed New Medical Device Regulations for Europe (this weblink brings you to the &#8220;Medical Devices &#8211; Ongoing Revisions&#8221; page of the EUROPA website).]]></description>
										<content:encoded><![CDATA[<p>The Emergo Group issued a White Paper on 22 October 2012 in regard to the <strong><a href="http://ec.europa.eu/health/medical-devices/documents/revision/index_en.htm" target="_blank" rel="noopener noreferrer">26 September 2012 Proposed New Medical Device Regulations for Europe</a></strong> (this weblink brings you to the &#8220;Medical Devices &#8211; Ongoing Revisions&#8221; page of the EUROPA website).</p>
<p><span id="more-2795"></span></p>
<p>&nbsp;</p>
<p>The <strong><a href="http://www.emergogroup.com/blog/2012/10/overview-new-medical-device-regulations-europe?utm_source=newsletter&amp;utm_medium=email&amp;utm_content=europe&amp;utm_campaign=october2012" target="_blank" rel="noopener noreferrer">Emergo blog posting</a></strong> says &#8220;While the European medical device regulatory system remains largely intact, greater detail has been added, and new mechanisms exist to bolster the weaknesses.&#8221; An example, is that in the existing MDD there are only 14 definitions while in the proposed Regulation there are now 50 definitions.  As you can see from this example the intent is to clarify the regulation so it is better understood. The Emergo <strong><a href="http://www.emergogroup.com/blog/2012/10/overview-new-medical-device-regulations-europe?utm_source=newsletter&amp;utm_medium=email&amp;utm_content=europe&amp;utm_campaign=october2012" target="_blank" rel="noopener noreferrer">blog post</a></strong> summarizes the high level primary changes while the <strong><a href="http://www2.emergogroup.com/white-paper-europe-proposed-regulation" target="_blank" rel="noopener noreferrer">Emergo White Paper</a></strong> goes into a much deeper analysis.</p>
<p>If you are interested in consulting support  from Eisner Safety Consultants to help you through this transition, closer to when finalized, or for current MDD or AIMDD please feel free to contact us via the information at our <strong><a href="http://www.eisnersafety.com/contact_eisner_safety/">contact us</a></strong> webpage.</p>
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