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	<title>Tissues of Animal Origin &#8211; Eisner Safety Consultants</title>
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		<title>Medical Devices Utilizing Tissues of Animal Origin New EU Commission Regulation</title>
		<link>https://eisnersafety.com/2012/08/30/medical-devices-utilizing-tissues-of-animal-origin-new-eu-commission-regulation/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=medical-devices-utilizing-tissues-of-animal-origin-new-eu-commission-regulation</link>
		
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		<pubDate>Thu, 30 Aug 2012 03:39:08 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[722/2012]]></category>
		<category><![CDATA[Active Implantable Medical Devices Directive]]></category>
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		<category><![CDATA[animal origin]]></category>
		<category><![CDATA[blog]]></category>
		<category><![CDATA[commission regulation]]></category>
		<category><![CDATA[Commission Regulation 722/2012]]></category>
		<category><![CDATA[EU]]></category>
		<category><![CDATA[EU Active Implantable Medical Device Directive]]></category>
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		<category><![CDATA[EU Commission]]></category>
		<category><![CDATA[EU Commission Regulation 722/2012]]></category>
		<category><![CDATA[EU MDD]]></category>
		<category><![CDATA[EU Medical Device Directive]]></category>
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		<category><![CDATA[Materials from Animal Sources]]></category>
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		<category><![CDATA[official journal of the european union]]></category>
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		<category><![CDATA[tissues]]></category>
		<category><![CDATA[Tissues of Animal Origin]]></category>
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					<description><![CDATA[This post is on the newly published Commission Regulation (EU) No 722/2012 of 8 August 2012 &#8220;concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured]]></description>
										<content:encoded><![CDATA[<p>This post is on the newly published <a href="http://www.eisnersafety.com/wp-content/uploads/2012/08/EU-Commission-Reg-722_2012-concerning-active-med-dvcs-med-dvcs-mfred-utilising-tissues-of-animal-origin.pdf">Commission Regulation (EU) No 722/2012</a> of 8 August 2012 &#8220;concerning particular requirements as regards the requirements laid down in Council Directives 90/385/EEC and 93/42/EEC with respect to active implantable medical devices and medical devices manufactured utilising tissues of animal origin&#8221; which was published in the Official Journal of the European Union on 9 August 2012.</p>
<p><span id="more-2676"></span><br />
<a href="http://www.medicaldeviceslegal.com/2012/08/27/new-eu-rules-for-active-medical-devices-utilising-non-viable-tissues-of-animal-origin/">The post on this Commission Regulation (EU) No 722/2012</a> is thx to Erik Vollebregt <a href="http://www.medicaldeviceslegal.com/" target="_blank" rel="noopener noreferrer">who blogs on EU legal and regulatory developments of medical devices</a>.  Erik has provided content previously to our blog and we thank him for his generosity in allowing us to post his content.</p>
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