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	<title>Apr 2021 &#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>Apr 2021 &#8211; Eisner Safety Consultants</title>
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		<title>EU Commission MDR &#038; IVDR Standardization Request List &#8211; Will it Succeed?</title>
		<link>https://eisnersafety.com/2021/04/21/eu-commission-mdr-ivdr-standardization-request-list-will-it-succeed/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=eu-commission-mdr-ivdr-standardization-request-list-will-it-succeed</link>
		
		<dc:creator><![CDATA[leoeisner]]></dc:creator>
		<pubDate>Wed, 21 Apr 2021 21:03:20 +0000</pubDate>
				<category><![CDATA[14971]]></category>
		<category><![CDATA[60601 Amendments]]></category>
		<category><![CDATA[60601 Series]]></category>
		<category><![CDATA[60601-1]]></category>
		<category><![CDATA[60601-1 A2]]></category>
		<category><![CDATA[60601-1 Amendment 2]]></category>
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		<category><![CDATA[60601-1-8]]></category>
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		<category><![CDATA[Apr 2021]]></category>
		<category><![CDATA[EU]]></category>
		<category><![CDATA[EU Commission]]></category>
		<category><![CDATA[Harmonized Standards]]></category>
		<category><![CDATA[MDCG]]></category>
		<category><![CDATA[MDD]]></category>
		<category><![CDATA[MDR]]></category>
		<category><![CDATA[Medical Device Regulation]]></category>
		<category><![CDATA[Notified Bodies]]></category>
		<category><![CDATA[State of the Art]]></category>
		<category><![CDATA[EN ISO 14971]]></category>
		<category><![CDATA[EN60601-1-11]]></category>
		<category><![CDATA[harmonized standards]]></category>
		<category><![CDATA[ISO 14971]]></category>
		<category><![CDATA[ISO 14971:2019]]></category>
		<category><![CDATA[IVDR]]></category>
		<category><![CDATA[IVDR 2017/746]]></category>
		<category><![CDATA[MDCG 2021-5]]></category>
		<category><![CDATA[MDR 2017/745]]></category>
		<guid isPermaLink="false">https://eisnersafety.com/?p=6888</guid>

					<description><![CDATA[COMMISSION IMPLEMENTATION DECISION M/575 was issued 14 April 2021: This is a list of standards the EU Commission is hoping to Harmonize under MDR and IVDR.&#160; One of the issues is the HAS consultant has issued a negative assessment on]]></description>
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<figure class="wp-block-gallery columns-1 is-cropped wp-block-gallery-1 is-layout-flex wp-block-gallery-is-layout-flex"><ul class="blocks-gallery-grid"><li class="blocks-gallery-item"><figure><img fetchpriority="high" decoding="async" width="1024" height="497" src="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2020/02/EU-Flags-for-Screen-1024x497.jpg" alt="" data-id="46" data-full-url="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2020/02/EU-Flags-for-Screen.jpg" data-link="https://eisnersafety.com/eu-flags-for-screen/" class="wp-image-46" srcset="https://eisnersafety.com/wp-content/uploads/2020/02/EU-Flags-for-Screen-1024x497.jpg 1024w, https://eisnersafety.com/wp-content/uploads/2020/02/EU-Flags-for-Screen-600x291.jpg 600w, https://eisnersafety.com/wp-content/uploads/2020/02/EU-Flags-for-Screen-300x146.jpg 300w, https://eisnersafety.com/wp-content/uploads/2020/02/EU-Flags-for-Screen-768x373.jpg 768w, https://eisnersafety.com/wp-content/uploads/2020/02/EU-Flags-for-Screen.jpg 1400w" sizes="(max-width: 1024px) 100vw, 1024px" /></figure></li></ul></figure>



<p class="has-medium-font-size"><a rel="noreferrer noopener" aria-label=" (opens in a new tab)" href="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2021/04/M575-EN-EU-Commission-StandaizationRequest-to-CEN-CENELEC-for-MDR-IVDR-14Apr2021.pdf" target="_blank">COMMISSION IMPLEMENTATION DECISION M/575</a> was issued 14 April 2021: This is a list of standards the EU Commission is <strong>hoping</strong> to Harmonize under MDR and IVDR.&nbsp; One of the issues is the HAS consultant has issued a negative assessment on EN ISO 14971 which the CEN/CLC JTC3 leadership is working with the HAS consultant to address the issues and to draft acceptable European annexes so Harmonization can occur for the standard.&nbsp; Many of the standards on the list in <a rel="noreferrer noopener" aria-label="M/575 (opens in a new tab)" href="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2021/04/M575-EN-EU-Commission-StandaizationRequest-to-CEN-CENELEC-for-MDR-IVDR-14Apr2021.pdf" target="_blank">M/575</a> reference to EN ISO 14971 so it is highly likely that CEN and CENELEC <strong><span style="text-decoration: underline;">will reject</span></strong> this newest version of the <a rel="noreferrer noopener" aria-label="EU Commission Standardization Request (opens in a new tab)" href="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2021/04/M575-EN-EU-Commission-StandaizationRequest-to-CEN-CENELEC-for-MDR-IVDR-14Apr2021.pdf" target="_blank">EU Commission Standardization Request</a> again and we won’t have any Harmonized Standards by the Date of Application (26 May 2021) for the MDR which will cause lots of problems for manufacturers and Notified Bodies and cause more delays for the MDR &amp; likely even for the IVDR I’m sorry to say.&nbsp; Also, the <a rel="noreferrer noopener" aria-label="MDDCG 2021-5 &quot;Guidance on standardisation for medical devices&quot; (opens in a new tab)" href="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2021/04/mdcg-2021-5-Guidance-on-Standization-for-medical-devices.pdf" target="_blank">MDCG 2021-5 &#8220;Guidance on standardisation for medical devices&#8221;</a> doesn’t seem to clarify when harmonized standards are not published through the Offical Journal of the EU what to do.&nbsp; In section 3.1 mentions Harmonized standards are voluntary with respect to the MDR &amp; IVDR as they were for the MDD, AIMDD, &amp; IVDD.&nbsp; The closest the <a rel="noreferrer noopener" aria-label="MDCG (opens in a new tab)" href="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2021/04/mdcg-2021-5-Guidance-on-Standization-for-medical-devices.pdf" target="_blank">MDCG</a> gets to it is to use the “State of Art” standards approach in section 3.5.</p>



<p class="has-medium-font-size">Another important observation is all the newest versions of the General &amp; Collateral IEC 60601 Standards that were issued Summer of 2020 (EN versions were issued later in the year) are listed in Annex I of the <a rel="noreferrer noopener" aria-label=" (opens in a new tab)" href="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2021/04/M575-EN-EU-Commission-StandaizationRequest-to-CEN-CENELEC-for-MDR-IVDR-14Apr2021.pdf" target="_blank">EU Commission Standardization Reques</a><a href="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2021/04/M575-EN-EU-Commission-StandaizationRequest-to-CEN-CENELEC-for-MDR-IVDR-14Apr2021.pdf" target="_blank" rel="noreferrer noopener" aria-label=" (opens in a new tab)">t</a> as the deadline to adopt these standards by 27 May 2024 &#8212; These are EN 60601-1, ed. 3.2; EN 60601-1-2, ed. 4.1; EN 60601-1-3, ed. 2.2; EN 60601-1-6, ed. 3.2; EN 60601-1-8, ed. 2.2; EN 60601-1-9, ed. 1.2; EN 60601-1-10, ed. 1.2; EN 60601-1-11, ed. 2.1; &amp; EN 60601-1-12, ed. 1.1 – The Particular Standards EN 60601-2-XX or EN ISO 80601-2-XX listed are primarily based on the previous versions of the General &amp; Collaterals of IEC 60601 standards on the <a rel="noreferrer noopener" aria-label="M/575 (opens in a new tab)" href="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2021/04/M575-EN-EU-Commission-StandaizationRequest-to-CEN-CENELEC-for-MDR-IVDR-14Apr2021.pdf" target="_blank">M/575</a> list so this will likely cause conflicts vs the listed new standards mentioned here.</p>



<p class="has-medium-font-size">Follow the full discussion and updates to this post on <a rel="noreferrer noopener" aria-label="LinkedIn (opens in a new tab)" href="https://www.linkedin.com/posts/leoeisnersafetyconsultants_eu-commission-mdr-ivdr-standardization-activity-6790743900513542144-KCQM" target="_blank">LinkedIn</a></p>



<p class="has-medium-font-size">Confused this is what Eisner Safety Consultants experts deal with all the time for countries for these and many other standards, regulations, laws, directives, and more.  <a href="https://eisnersafety.com/about_us/associates/">Leo Eisner</a> is an expert on standards development and sit on many standards committees.  Let us help you through this process.  Need help with Essential Performance. Feel free to schedule a call with Leo www.EisnerSafety.com/Schedule-Call/ or contact Leo at&nbsp;&#76;&#101;o&#64;&#69;&#105;sn&#101;r&#83;&#97;f&#101;t&#121;&#46;com or through our contact form at <a href="https://eisnersafety.com/contact_eisner_safety/">https://eisnersafety.com/contact_eisner_safety/</a>.</p>
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			</item>
		<item>
		<title>IEC Article on IEC 60601 Series Amendments Project</title>
		<link>https://eisnersafety.com/2021/04/11/iec-article-on-iec-60601-series-amendments-project/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=iec-article-on-iec-60601-series-amendments-project</link>
		
		<dc:creator><![CDATA[leoeisner]]></dc:creator>
		<pubDate>Sun, 11 Apr 2021 23:15:59 +0000</pubDate>
				<category><![CDATA[60601 Amendments]]></category>
		<category><![CDATA[60601 Series]]></category>
		<category><![CDATA[60601-1]]></category>
		<category><![CDATA[60601-1 Amendment 2]]></category>
		<category><![CDATA[60601-1-2]]></category>
		<category><![CDATA[Apr 2021]]></category>
		<category><![CDATA[IEC]]></category>
		<category><![CDATA[InCompliance Magazine]]></category>
		<category><![CDATA[60601 series]]></category>
		<category><![CDATA[IEC 60601-1]]></category>
		<category><![CDATA[IEC60601-1]]></category>
		<guid isPermaLink="false">https://eisnersafety.com/?p=6885</guid>

					<description><![CDATA[A good summary article on IEC e-Tech News about the IEC 60601 Series Amendments project that published last summer (2020) the General 60601-1, and Collateral standards (60601-1-XX).  Please note that you need to read further comments in some of my articles about IEC 60601-1 for IEC 62368-1 and IEC 60601-1-2 for some additional details.  One blog post is an article from InCompliance]]></description>
										<content:encoded><![CDATA[
<figure class="wp-block-image size-large"><img decoding="async" width="1024" height="497" src="https://eisnersafety.com/eisnersafetycom/wp-content/uploads/2020/02/slide06-1024x497.jpg" alt="" class="wp-image-48" srcset="https://eisnersafety.com/wp-content/uploads/2020/02/slide06-1024x497.jpg 1024w, https://eisnersafety.com/wp-content/uploads/2020/02/slide06-600x291.jpg 600w, https://eisnersafety.com/wp-content/uploads/2020/02/slide06-300x146.jpg 300w, https://eisnersafety.com/wp-content/uploads/2020/02/slide06-768x373.jpg 768w, https://eisnersafety.com/wp-content/uploads/2020/02/slide06.jpg 1400w" sizes="(max-width: 1024px) 100vw, 1024px" /></figure>



<p class="has-medium-font-size">A good summary article on <a href="https://etech.iec.ch/issue/2020-05/iec-publishes-amendments-to-key-medical-device-standards">IEC e-Tech News</a> about the IEC 60601 Series Amendments project that published last summer (2020) the General 60601-1, and Collateral standards (60601-1-XX).  <strong>Please note</strong> that you need to read further comments in some of my articles about IEC 60601-1 for IEC 62368-1 and IEC 60601-1-2 for some additional details.  One blog post is an article from <a href="https://eisnersafety.com/2020/11/16/iec-60601-amendments-updates-have-published-changes-and-impacts/">InCompliance</a></p>
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