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		<title>BiotechBistro Forums Tag: QSR</title>
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		<description>The Business of Biotechnology</description>
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		<pubDate>Fri, 10 Sep 2010 19:20:40 +0000</pubDate>
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			<title>javellan on "Two FDA Quality Systems Compliance Resources Published"</title>
			<link>http://biotechbistro.com/forum/topic/two-fda-quality-systems-compliance-resources-published#post-9</link>
			<pubDate>Fri, 20 Feb 2009 16:11:11 +0000</pubDate>
			<dc:creator>javellan</dc:creator>
			<guid isPermaLink="false">9@http://biotechbistro.com/forum/</guid>
			<description>&#60;p&#62;Two new FDA quality systems compliance resources – &#60;strong&#62;Bulletproof Yourself against FDA Enforcement&#60;/strong&#62; and &#60;strong&#62;FDA Quality Systems Records Requirements for GLPs, GCPs, GMPs&#60;/strong&#62; – have been published by the SmarterCompliance™ newsletter and Cerulean Associates LLC.&#60;/p&#62;
&#60;p&#62;Both publications combine recorded executive teleseminars with resource kits of checklists, templates, example FDA warning letters, and other reference material designed to ease implementation of various recommendations and expert advice.&#60;/p&#62;
&#60;p&#62;&#60;strong&#62;Bulletproof Yourself against FDA Enforcement&#60;/strong&#62; builds on Cerulean’s in-depth industry report from last year, FDA Enforcement Trends 2008-2009, and adds a review of the top 10 agency inspection priorities for domestic US and international sites, four detailed self-assessment checklists, a step-by-step strategy for ensuring positive inspection outcomes, three article reprints, and an hour-long audio-visual analysis of the FDA priorities for 2009 along with recommendations to stay off the FDA radar screen for the next 12-18 months.  Also included is a complimentary copy of the industry report, FDA Enforcement Trends 2008-2009.&#60;/p&#62;
&#60;p&#62;&#60;strong&#62;FDA Quality Systems Records Requirements&#60;/strong&#62; includes a 9-page matrix of FDA records and documentation requirements for firms during GLPs, GCPs, and GMPs, an 11-step strategy overview guide, several self-assessment checklists, a policy framework template, multiple article reprints, and other reference materials.  Also included is an hour-length audio-visual recording of last week’s executive teleconference with questions and answers from the audience.&#60;/p&#62;
&#60;p&#62;Both resource kit publications are available – either in download format or CD and hard copy – through the Cerulean website at &#60;a href=&#34;http://www.ceruleanllc.com&#34; rel=&#34;nofollow&#34;&#62;http://www.ceruleanllc.com&#60;/a&#62;.&#60;/p&#62;
&#60;p&#62;Cerulean’s next online seminar for executives, &#60;strong&#62;Frugal FDA Compliance:  Getting More Done with Less&#60;/strong&#62;, is scheduled for Tuesday, March 24.  Want to attend?  Visit &#60;a href=&#34;http://www.ceruleanllc.com/webinar&#34; rel=&#34;nofollow&#34;&#62;http://www.ceruleanllc.com/webinar&#60;/a&#62; to learn more and register.&#60;/p&#62;
&#60;p&#62;Cerulean Associates LLC is a private advisory company that helps executives in the pharmaceutical, biotech and device sectors cut costs, streamline quality systems, speed new drug, biologic or device time to market, and protect their intellectual property from theft.  Cerulean publishes the SmarterCompliance™ newsletter as part of its SmarterCompliance FDA executive advisory program.  On the web at &#60;a href=&#34;http://www.ceruleanllc.com&#34; rel=&#34;nofollow&#34;&#62;http://www.ceruleanllc.com&#60;/a&#62;.&#60;/p&#62;
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