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	<title>The Medicines and Healthcare products Regulatory Agency &#8211; Eisner Safety Consultants</title>
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	<description>Regulatory &#38; Safety Experts for Global Medical Device Approvals</description>
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	<title>The Medicines and Healthcare products Regulatory Agency &#8211; Eisner Safety Consultants</title>
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		<title>UK MHRA Guidance on EU Regulation 207/2012 on electronic labeling of med dvcs</title>
		<link>https://eisnersafety.com/2013/05/06/uk-mhra-guidance-on-eu-regulation-2072012-on-electronic-labeling-of-med-dvcs/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=uk-mhra-guidance-on-eu-regulation-2072012-on-electronic-labeling-of-med-dvcs</link>
		
		<dc:creator><![CDATA[leoeisner]]></dc:creator>
		<pubDate>Mon, 06 May 2013 04:41:22 +0000</pubDate>
				<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[207/2012]]></category>
		<category><![CDATA[E-Label]]></category>
		<category><![CDATA[Electronic Label]]></category>
		<category><![CDATA[Electronic Labeling]]></category>
		<category><![CDATA[Electronic Labelling]]></category>
		<category><![CDATA[EU Commission]]></category>
		<category><![CDATA[Guidance]]></category>
		<category><![CDATA[Guidance on electronic labeling]]></category>
		<category><![CDATA[Guidance on electronic labeling of medical devices]]></category>
		<category><![CDATA[Guidance on electronic labelling]]></category>
		<category><![CDATA[Guidance on electronic labelling of medical devices]]></category>
		<category><![CDATA[Medical Devices]]></category>
		<category><![CDATA[MHRA]]></category>
		<category><![CDATA[The Medicines and Healthcare products Regulatory Agency]]></category>
		<category><![CDATA[UK MHRA]]></category>
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					<description><![CDATA[On 9 Jan 2013 the UK MHRA (The Medicines and Healthcare products Regulatory Agency) released a Guidance on EU Commission Regulation 207/2012 on electronic labeling of medical devices.  This regualtion came into force on 1 March 2013 so you can]]></description>
										<content:encoded><![CDATA[<p><span style="font-size: small; font-family: arial, helvetica, sans-serif;">On 9 Jan 2013 the UK MHRA (The Medicines and Healthcare products Regulatory Agency) released a Guidance on EU Commission Regulation 207/2012 on electronic labeling of medical devices.  This regualtion came into force on 1 March 2013 so you can rely on this guidance to help you meet the regulation.  The UK MHRA <strong><a href="http://www.mhra.gov.uk/Howweregulate/Devices/Devicesregulatorynews/CON222581" target="_blank" rel="noopener noreferrer">webpage</a></strong> includes the text of their guidance for how to apply the requirements of 207/2012 on electronic labeling of medical devices.</span></p>
<p><span style="font-family: arial, helvetica, sans-serif; font-size: small;">Past posts to refer to includes:</span></p>
<ul>
<li><strong><a href="http://www.EisnerSafety.com/electronic-ifus-for-eu-mdd-aimdd-devices/" target="_blank" rel="noopener noreferrer">Electronic IFUs for EU MDD &amp; AIMDD Devices</a></strong></li>
<li><strong><a href="http://www.EisnerSafety.com/ec-publishes-draft-regulation-on-electronic-ifus-of-medical-devices/" target="_blank" rel="noopener noreferrer">EC publishes draft regulation on electronic IFUs of Medical Devices</a></strong></li>
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