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	<title>General Controls - Revision history</title>
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	<updated>2026-10-25T10:12:45Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://wiki.dirkjanswagerman.nl/index.php?title=General_Controls&amp;diff=574&amp;oldid=prev</id>
		<title>Dirkjan: Created page with &quot;In FDA regulation, general controls include: # An establishments FDA registration form FDA 2891 # Product listing form FDA 2892 # Compliance with FDA...&quot;</title>
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		<updated>2020-08-25T07:19:40Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;In FDA regulation, general controls include: # An establishments FDA registration form &lt;a href=&quot;/index.php?title=FDA_2891&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;FDA 2891 (page does not exist)&quot;&gt;FDA 2891&lt;/a&gt; # Product listing form &lt;a href=&quot;/index.php?title=FDA_2892&amp;amp;action=edit&amp;amp;redlink=1&quot; class=&quot;new&quot; title=&quot;FDA 2892 (page does not exist)&quot;&gt;FDA 2892&lt;/a&gt; # Compliance with FDA...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;In FDA regulation, general controls include:&lt;br /&gt;
# An establishments FDA registration form [[FDA 2891|FDA 2891]]&lt;br /&gt;
# Product listing form [[FDA 2892|FDA 2892]]&lt;br /&gt;
# Compliance with FDA&amp;#039;s [[Good Manufacturing Practice|Good Manufacturing Practice]] regulation, now called [[Quality System Regulations|Quality System Regulations]]&lt;br /&gt;
# Adverse reporting or FDA&amp;#039;s [[Medical Device Reporting Regulations|Medical Device Reporting Regulations]]&lt;br /&gt;
[[Category:fda]]&lt;br /&gt;
&lt;br /&gt;
[[Category:FDA]]&lt;br /&gt;
&lt;br /&gt;
[[Category:Term]]&lt;/div&gt;</summary>
		<author><name>Dirkjan</name></author>
		
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