<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Equivalency Agreement &#8211; Veraque</title>
	<atom:link href="https://veraqueconsulting.cn/category/equivalency-agreement/feed/" rel="self" type="application/rss+xml" />
	<link>https://veraqueconsulting.cn</link>
	<description>我们满足您的需求</description>
	<lastBuildDate>Tue, 03 Mar 2020 18:19:13 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=6.8.1</generator>

<image>
	<url>https://veraqueconsulting.cn/wp-content/uploads/2019/11/cropped-logo-32x32.png</url>
	<title>Equivalency Agreement &#8211; Veraque</title>
	<link>https://veraqueconsulting.cn</link>
	<width>32</width>
	<height>32</height>
</image> 
	<item>
		<title>Equivalency Agreement summary</title>
		<link>https://veraqueconsulting.cn/2020/01/24/equivalency-agreement-summary/</link>
					<comments>https://veraqueconsulting.cn/2020/01/24/equivalency-agreement-summary/#respond</comments>
		
		<dc:creator><![CDATA[Miguel Torres]]></dc:creator>
		<pubDate>Fri, 24 Jan 2020 18:55:22 +0000</pubDate>
				<category><![CDATA[Equivalency Agreement]]></category>
		<category><![CDATA[equivalency agreement]]></category>
		<guid isPermaLink="false">https://veraqueconsulting.cn/?p=640</guid>

					<description><![CDATA[<p>&#160; Every controlled medical devices intended to be sold in Mexico must undergo a previous authorization by the Mexican Ministry of Health before its commercialization. The aforementioned authorization is a document called Sanitary Registration, which COFEPRIS (the Mexican FDA) issues after evaluating a set of requirements. In addition, there are two ways to obtain the [&#8230;]</p>
<p>The post <a rel="nofollow" href="https://veraqueconsulting.cn/2020/01/24/equivalency-agreement-summary/">Equivalency Agreement summary</a> appeared first on <a rel="nofollow" href="https://veraqueconsulting.cn">Veraque</a>.</p>
]]></description>
										<content:encoded><![CDATA[<p><img decoding="async" class="alignnone wp-image-242" role="img" src="https://veraqueconsulting.cn/wp-content/uploads/2019/12/prvntion.svg" alt="" width="98" height="98" /></p>
<p>&nbsp;</p>
<p>Every controlled medical devices intended to be sold in Mexico must undergo a previous authorization by the Mexican Ministry of Health before its commercialization. The aforementioned authorization is a document called Sanitary Registration, which <a href="https://www.gob.mx/cofepris" target="_blank" rel="noopener noreferrer">COFEPRIS</a> (the Mexican FDA) issues after evaluating a set of requirements.</p>
<p>In addition, there are <strong>two ways</strong> to obtain the Sanitary Registration:</p>
<p>The <em><a href="https://www.gob.mx/cofepris/acciones-y-programas/registro-de-dispositivos-medicos-nuevos" target="_blank" rel="noopener noreferrer">ordinary process</a></em> and the <em>equivalency agreement.</em></p>
<p>On the other hand, COFEPRIS has determined that the requirements to get the Sanitary Registration of a medical device in Mexico by the ordinary process are similar (<em>Equivalent</em>) to that needed for approval of a medical device in the <a href="http://dof.gob.mx/nota_detalle.php?codigo=5164641&amp;fecha=26/10/2010" target="_blank" rel="noopener noreferrer">United States of America, Canada</a> or <a href="http://www.dof.gob.mx/nota_detalle.php?codigo=5231033&amp;fecha=25/01/2012" target="_blank" rel="noopener noreferrer">Japan</a> respectively. Hence COFEPRIS created the <strong>equivalency agreements.</strong></p>
<p>In order to be eligible to apply for the <strong>equivalency agreement </strong>route, a series of requirements must be fulfilled. The most important is to hold a valid approval from either the <a href="https://www.fda.gov/medical-devices" target="_blank" rel="noopener noreferrer">Food and Drug Administration (FDA)</a>, <a href="https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices.html" target="_blank" rel="noopener noreferrer">Health Canada</a> or <a href="https://www.pmda.go.jp/english/index.html" target="_blank" rel="noopener noreferrer">the Ministry of Health Welfare and Labor</a> depending on which country the medical device has been approved for its marketing.</p>
<p>There are many perks of requesting a sanitary registry through the equivalency agreement pathway, specifically:</p>
<ul>
<li>Less technical and legal documentation is requested by COFEPRIS.</li>
<li>The review and approval times are shorter</li>
<li>Reduced translation costs.</li>
</ul>
<p>However, the equivalency agreement is not exempt of drawbacks. For instance, it could be harder to get the medical device approved in one of the countries listed above.</p>
<p>In addition, the rules in these countries may change and gather the right documentation to be submitted to COFEPRIS can be complicated or time consuming.</p>
<p>It is important to notice that this kind of requests are not eligible to be reviewed by an authorized <a href="https://veraqueconsulting.cn/ultimate-guide-for-regulatory-affairs-in-mexico/" target="_blank" rel="noopener noreferrer">third party</a>. Therefore, COFEPRIS will review them directly with more strict criteria and the documents and information submitted must be correct to avoid delays and take advantage of this fast track route.</p>
<p><strong>Check similar notes in our <a href="https://veraqueconsulting.cn/guides/" target="_blank" rel="noopener noreferrer">Guides</a>.</strong></p>
<p><em>We want to thank <a href="https://www.linkedin.com/in/hugo-vite-a2807380/" target="_blank" rel="noopener noreferrer">Hugo Vite</a> for his support on writing this document.</em></p>
<p>The post <a rel="nofollow" href="https://veraqueconsulting.cn/2020/01/24/equivalency-agreement-summary/">Equivalency Agreement summary</a> appeared first on <a rel="nofollow" href="https://veraqueconsulting.cn">Veraque</a>.</p>
]]></content:encoded>
					
					<wfw:commentRss>https://veraqueconsulting.cn/2020/01/24/equivalency-agreement-summary/feed/</wfw:commentRss>
			<slash:comments>0</slash:comments>
		
		
			</item>
	</channel>
</rss>
