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	<id>https://wiki.dirkjanswagerman.nl/index.php?action=history&amp;feed=atom&amp;title=ISO13485_-_5.1_Management_commitment</id>
	<title>ISO13485 - 5.1 Management commitment - Revision history</title>
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	<updated>2026-10-25T12:12:34Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wiki.dirkjanswagerman.nl/index.php?title=ISO13485_-_5.1_Management_commitment&amp;diff=3219&amp;oldid=prev</id>
		<title>Dirkjan: Created page with &quot;&#039;&#039;&#039;5.1 Management commitment&#039;&#039;&#039;  Top management shall provide evidence of its commitment to the development and implementation of the quality management system and maintaining...&quot;</title>
		<link rel="alternate" type="text/html" href="https://wiki.dirkjanswagerman.nl/index.php?title=ISO13485_-_5.1_Management_commitment&amp;diff=3219&amp;oldid=prev"/>
		<updated>2020-08-25T09:46:00Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;&amp;#039;&amp;#039;&amp;#039;5.1 Management commitment&amp;#039;&amp;#039;&amp;#039;  Top management shall provide evidence of its commitment to the development and implementation of the quality management system and maintaining...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;5.1 Management commitment&amp;#039;&amp;#039;&amp;#039;&lt;br /&gt;
&lt;br /&gt;
Top management shall provide evidence of its commitment to the development and implementation of the quality management system and maintaining its effectiveness by&lt;br /&gt;
a) communicating to the organization the importance of meeting customer as well as statutory and regulatory requirements,&lt;br /&gt;
b) establishing the quality policy,&lt;br /&gt;
c) ensuring that quality objectives are established,&lt;br /&gt;
d) conducting management reviews, and&lt;br /&gt;
e) ensuring the availability of resources&lt;br /&gt;
&lt;br /&gt;
NOTE For the purposes of this International Standard, statutory requirements are limited to the safety and performance of the medical device only.&lt;br /&gt;
[[Category:quality]]&lt;br /&gt;
&lt;br /&gt;
[[Category:ISO13485]]&lt;/div&gt;</summary>
		<author><name>Dirkjan</name></author>
		
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