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	<title>User Fees &#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>FDA Guidance &#038; Fed Reg &#8211; FY 2011 Med Dvc User Fee Rates</title>
		<link>https://eisnersafety.com/2010/08/10/fda-guidance-fed-reg-fy-2011-med-dvc-user-fee-rates/?utm_source=rss&#038;utm_medium=rss&#038;utm_campaign=fda-guidance-fed-reg-fy-2011-med-dvc-user-fee-rates</link>
		
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		<pubDate>Tue, 10 Aug 2010 18:46:56 +0000</pubDate>
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					<description><![CDATA[FDA Guidance Fiscal Year 2011 Medical Device User Fee Small Business Qualification &#38; Certification http://ht.ly/2nHdQ &#38; Federal Register Medical Device User Fee Rates Fiscal Year 2011 http://ht.ly/2nHgX]]></description>
										<content:encoded><![CDATA[<p>FDA Guidance Fiscal Year 2011 Medical Device User Fee Small Business Qualification &amp; Certification <a rel="nofollow" href="http://ht.ly/2nHdQ">http://ht.ly/2nHdQ</a> &amp;  Federal Register Medical Device User Fee Rates Fiscal Year 2011 <a rel="nofollow" href="http://ht.ly/2nHgX">http://ht.ly/2nHgX</a></p>
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		<title>Health Canada Proposed Increases of User Fees for Medical Devices &#038; Drugs Tabled on 4/12/2010</title>
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		<pubDate>Wed, 26 May 2010 00:41:51 +0000</pubDate>
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					<description><![CDATA[Health Canada Proposed Increases of User Fees for Medical Devices and Drugs was tabled on 4/12/2010 http://ht.ly/1PSFF]]></description>
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		<title>Draft FDA Guidance on User Fees</title>
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		<pubDate>Tue, 04 Aug 2009 00:00:37 +0000</pubDate>
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					<description><![CDATA[Guidance for Industry and FDA: User Fees and Refunds for Premarket Approval Applications A draft guidance has been issued for comment purposes only, see &#8220;Draft Guidance for Industry and FDA Staff: User Fees and Refunds for Premarket Approval Applications&#8221; issued]]></description>
										<content:encoded><![CDATA[<h3><a href="http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm089744.htm" target="_blank" rel="noopener noreferrer">Guidance for Industry and FDA: User Fees and Refunds for Premarket Approval Applications</a></h3>
<p>A draft guidance has been issued for comment purposes only, see &#8220;<a href="http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm119809.htm" target="_blank" rel="noopener noreferrer">Draft Guidance for Industry and FDA Staff: User Fees and Refunds for Premarket Approval Applications</a>&#8221; issued March 13, 2009, which if issued as final, will replace the currently available guidance which was issued on November 24, 2003.</p>
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