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	<rss version="2.0"> <channel> <title>Most Popular White Papers and WebcastsMedical Software Research</title> 
	<link>http://www.bitpipe.com/tlist/Medical-Software.html?asrc=RSS_BP </link> <description>White papers, webcasts,
	podcasts, IT downloads and product information provided by Bitpipe</description>
	<language>en-us</language> <lastBuildDate>Tue, 25 Aug 2009 16:15:25 EDT</lastBuildDate>
	<pubDate>Tue, 25 Aug 2009 16:15:25 EDT</pubDate>  <item> <title><![CDATA[Geisinger Health System Selects Kofax Intelligent Capture & Exchange to Automate Medical Records Processing]]></title> <link><![CDATA[http://www.bitpipe.com/detail/RES/1251230138_188.html?asrc=RSS_BP_TERM]]></link>
		<description><![CDATA[
    This case study will take a look at how Geisinger Health System worked with Kofax Intelligent Capture and Exchange to manage a rapidly growing amount of data at multiple locations.  By upgrading to Kofax Capture 5, Geisinger Health System was able to scan high resolution copies of patient records into the workflow and access them at any location.
   Published by: Kofax, Inc.]]></description>
		<pubDate>Tue, 25 Aug 2009 24:00:00 EDT</pubDate> </item>  <item> <title><![CDATA[Proactively Controlling Access to Patient Data]]></title> <link><![CDATA[http://www.bitpipe.com/detail/RES/1248791510_534.html?asrc=RSS_BP_TERM]]></link>
		<description><![CDATA[
    In a typical healthcare organization, hundreds to thousands of medical and support staff need to access patient data to do their job. How do you effectively enforce access controls to hospital information systems without hampering medical care efficiency and effectiveness?  Read this paper and learn how.
   Published by: FoxT]]></description>
		<pubDate>Wed, 01 Jul 2009 24:00:00 EDT</pubDate> </item>  <item> <title><![CDATA[In my Defense let me State that the Bed was Already on Fire when I climbed into it -- A Guide for Medical Device Developers to design better products, save money, and meet FDA/CDRH requirements]]></title> <link><![CDATA[http://www.bitpipe.com/detail/RES/1242240837_65.html?asrc=RSS_BP_TERM]]></link>
		<description><![CDATA[
    The CDRH (Center for Devices and Radiological Health) is in the process of updating their standards and suggested practices. They are going to be more strict with medical device developers. The purpose of this paper is to present the medical device developer guidelines for complying with the &quot;suggestions&quot; of the CDRH.
   Published by: IBM]]></description>
		<pubDate>Tue, 31 Mar 2009 24:00:00 EDT</pubDate> </item>  </channel> </rss>

