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	<title>EDA &#187; Video</title>
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	<description>Electronic Design Automation (EDA) tools span the entire design chain for electronics products. Automation starts with technology computer-aided automation (TCAD) tools, which engineers use to model the fabrication processes that determine device physical behavior. Modeling engineers convert that behavior to simulation models, which designers then use to analyze their circuits, from individual transistors and analog circuits to logic gates, to complex digital blocks and complete integrated circuits (ICs) and systems. Physical implementation tools are used to layout chips, packages and printed-circuit boards (PCBs) for manufacturing. Verification tools are critical for engineers to test their designs for correct functional operation, including the effects of environmental factors such as variations in temperature, voltage and manufacturing tolerances.</description>
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		<title>What&#8217;s Hot at DAC 2011</title>
		<link>http://www.youtube.com/watch?v=Y4BCHAIe8yQ&#038;feature=youtube_gdata</link>
		<comments>http://www.youtube.com/watch?v=Y4BCHAIe8yQ&#038;feature=youtube_gdata#comments</comments>
		<pubDate>Wed, 31 Aug 2011 19:20:32 +0000</pubDate>
		<dc:creator>DACPavilion</dc:creator>
				<category><![CDATA[Video]]></category>
		<category><![CDATA[DAC San Diego]]></category>
		<category><![CDATA[Gary Smith]]></category>
		<category><![CDATA[Pavilion Panel]]></category>
		<category><![CDATA[What's Hot at DAC]]></category>

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		<description><![CDATA[Gary Smith of Gary Smith EDA talks about the trends and what's hot at DAC 2011. Gary opens the Pavilion Program on Monday, June 6th at 9:15AM.]]></description>
			<content:encoded><![CDATA[<p>Gary Smith of Gary Smith EDA talks about the trends and what&#8217;s hot at DAC 2011. Gary opens the Pavilion Program on Monday, June 6th at 9:15AM.</p>
]]></content:encoded>
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		<title>DAC 2011 Women in Electronic Design Pavilion Panel</title>
		<link>http://www.youtube.com/watch?v=nssIb6fLr2Q&#038;feature=youtube_gdata</link>
		<comments>http://www.youtube.com/watch?v=nssIb6fLr2Q&#038;feature=youtube_gdata#comments</comments>
		<pubDate>Wed, 31 Aug 2011 18:25:46 +0000</pubDate>
		<dc:creator>hollystump1</dc:creator>
				<category><![CDATA[Video]]></category>
		<category><![CDATA[DAC 2011]]></category>
		<category><![CDATA[http://gdata.youtube.com/schemas/2007#playlist]]></category>
		<category><![CDATA[Tech]]></category>
		<category><![CDATA[Women in Electronics]]></category>
		<category><![CDATA[WWED]]></category>

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		<description><![CDATA[This DAC 2011 Pavilion Panel, Is all about your career.....women and  men, in both  electronics and in EDA....
Career Velocity Vectors:  The Excitement of Electrical engineering and computer science! 
Brought to you by Women in Electronic Design.
Pleas...]]></description>
			<content:encoded><![CDATA[<p>This DAC 2011 Pavilion Panel, Is all about your career&#8230;..women and  men, in both  electronics and in EDA&#8230;.<br />
Career Velocity Vectors:  The Excitement of Electrical engineering and computer science!<br />
Brought to you by Women in Electronic Design.<br />
Please join us for this exciting Career panel in the Pavilion at Dac 2011, Monday June 6, 2011, in San Diego.</p>
]]></content:encoded>
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		</item>
		<item>
		<title>The Voices of DAC&#8211;It&#8217;s a wrap!</title>
		<link>http://www.youtube.com/watch?v=bjOiIrify5E&#038;feature=youtube_gdata</link>
		<comments>http://www.youtube.com/watch?v=bjOiIrify5E&#038;feature=youtube_gdata#comments</comments>
		<pubDate>Wed, 31 Aug 2011 18:25:46 +0000</pubDate>
		<dc:creator>SynopsysTV</dc:creator>
				<category><![CDATA[Video]]></category>
		<category><![CDATA[48th DAC]]></category>
		<category><![CDATA[Conversation Central]]></category>
		<category><![CDATA[Daniel Nenni]]></category>
		<category><![CDATA[Design Automation Conference]]></category>
		<category><![CDATA[Electronic Engineering Journal]]></category>
		<category><![CDATA[Karen Bartleson]]></category>
		<category><![CDATA[Kevin Morris]]></category>
		<category><![CDATA[The SemiWiki Project]]></category>

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		<description><![CDATA[Guests: Daniel Nenni, Founder, The SemiWiki Project and Kevin Morris, Editor, Electronic Engineering Journal
Host: Karen Bartleson, Sr. Director, Community Marketing, Synopsys

As the 48th Design Automation Conference came to a close, Daniel Nenni and ...]]></description>
			<content:encoded><![CDATA[<p>Guests: Daniel Nenni, Founder, The SemiWiki Project and Kevin Morris, Editor, Electronic Engineering Journal<br />
Host: Karen Bartleson, Sr. Director, Community Marketing, Synopsys</p>
<p>As the 48th Design Automation Conference came to a close, Daniel Nenni and Kevin Morris talked about what they saw, heard, learned, and observed about the 48th DAC. DAC is the premier conference of the electronic design industry and is known for announcements of technology advancements, new products, alliances and partnerships, and standards activities.</p>
<p>This show was originally streamed live to the Synopsys Facebook page at the 48th DAC.</p>
]]></content:encoded>
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		</item>
		<item>
		<title>Video: Reducing Manual Effort for Risk Management Compliance</title>
		<link>http://www.embedded-computing.com/articles/id/?5326</link>
		<comments>http://www.embedded-computing.com/articles/id/?5326#comments</comments>
		<pubDate>Fri, 19 Aug 2011 15:00:00 +0000</pubDate>
		<dc:creator>Staff at MKS, a PTC Company, MKS (ALM)</dc:creator>
				<category><![CDATA[Video]]></category>
		<category><![CDATA[510 k fda]]></category>
		<category><![CDATA[510 k premarket notification]]></category>
		<category><![CDATA[510 k submission]]></category>
		<category><![CDATA[510k fda]]></category>
		<category><![CDATA[510k fda approval]]></category>
		<category><![CDATA[510k medical device]]></category>
		<category><![CDATA[biomedical device companies]]></category>
		<category><![CDATA[class ii medical devices]]></category>
		<category><![CDATA[device fda]]></category>
		<category><![CDATA[devices fda]]></category>
		<category><![CDATA[diagnostic medical device]]></category>
		<category><![CDATA[embedded software]]></category>
		<category><![CDATA[engineering change and collaboration]]></category>
		<category><![CDATA[fda approval medical device]]></category>
		<category><![CDATA[fda approval medical devices]]></category>
		<category><![CDATA[fda class ii]]></category>
		<category><![CDATA[fda device]]></category>
		<category><![CDATA[fda device approval]]></category>
		<category><![CDATA[fda device classification]]></category>
		<category><![CDATA[fda device registration]]></category>
		<category><![CDATA[fda devices]]></category>
		<category><![CDATA[fda medical device]]></category>
		<category><![CDATA[fda medical device listing]]></category>
		<category><![CDATA[fda medical device registration]]></category>
		<category><![CDATA[fda medical devices]]></category>
		<category><![CDATA[fda registration]]></category>
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		<category><![CDATA[fda regulatory]]></category>
		<category><![CDATA[fda regulatory affairs]]></category>
		<category><![CDATA[fda regulatory consultant]]></category>
		<category><![CDATA[fda regulatory consultants]]></category>
		<category><![CDATA[fda regulatory requirements]]></category>
		<category><![CDATA[fda submission]]></category>
		<category><![CDATA[fda submissions]]></category>
		<category><![CDATA[manufacturing medical device]]></category>
		<category><![CDATA[manufacturing medical devices]]></category>
		<category><![CDATA[medical device]]></category>
		<category><![CDATA[medical device diagnostic]]></category>
		<category><![CDATA[medical device fda]]></category>
		<category><![CDATA[medical device fda approval]]></category>
		<category><![CDATA[medical device manufacturers]]></category>
		<category><![CDATA[medical device manufacturing]]></category>
		<category><![CDATA[medical device manufacturing companies]]></category>
		<category><![CDATA[medical device manufacturing industry]]></category>
		<category><![CDATA[medical device reimbursement]]></category>
		<category><![CDATA[Medical devices]]></category>
		<category><![CDATA[medical devices & diagnostics]]></category>
		<category><![CDATA[medical devices and diagnostics]]></category>
		<category><![CDATA[medical devices companies]]></category>
		<category><![CDATA[medical devices fda]]></category>
		<category><![CDATA[medical devices manufacturer]]></category>
		<category><![CDATA[medical devices manufacturers]]></category>
		<category><![CDATA[medical devices manufacturing]]></category>
		<category><![CDATA[medical devices regulation]]></category>
		<category><![CDATA[medical devices reimbursement]]></category>
		<category><![CDATA[medical diagnostic device]]></category>
		<category><![CDATA[mks (alm)]]></category>
		<category><![CDATA[premarket notification 510 k]]></category>
		<category><![CDATA[product development methodologies]]></category>
		<category><![CDATA[regulatory affairs fda]]></category>
		<category><![CDATA[reimbursement medical devices]]></category>
		<category><![CDATA[requirements management]]></category>
		<category><![CDATA[software development metrics]]></category>
		<category><![CDATA[software lifecycle process]]></category>
		<category><![CDATA[software process metrics]]></category>
		<category><![CDATA[streamline compliance]]></category>

		<guid isPermaLink="false">http://tech.opensystemsmedia.com/eda/?guid=0b5e41c74056884d6d946c678ddb291e</guid>
		<description><![CDATA[Hazard analysis and risk management are standard procedures that medical device companies must undertake as part of their compliance effort for FDA regulations and other standards. The challenge is that risks are typically managed manually and separately from control measures and other engineering lifecycle artifacts such as requirements and tests.]]></description>
			<content:encoded><![CDATA[<div id='story' class='body'>
<div class='body-text'></a>This solution overview provides a brief look at how Integrity, a PTC product (formerly MKS Integrity) reduces the effort in Risk Management for Medical Device Engineering companies.</p>
<p>Learn how by providing organizations with the ability to reduce the overwhelming complexity of developing software intensive products removes barriers which ultimately drives more innovative products into the market and help overcome the most commonly reported challenges in the Medical Device Industry.</p>
</div></div>
]]></content:encoded>
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		<item>
		<title>Video: Accelerating Software Innovation</title>
		<link>http://www.embedded-computing.com/articles/id/?5254</link>
		<comments>http://www.embedded-computing.com/articles/id/?5254#comments</comments>
		<pubDate>Mon, 25 Jul 2011 15:00:00 +0000</pubDate>
		<dc:creator>Video, MKS (ALM)</dc:creator>
				<category><![CDATA[Video]]></category>
		<category><![CDATA[application lifecycle management]]></category>
		<category><![CDATA[embedded software]]></category>
		<category><![CDATA[mks (alm)]]></category>
		<category><![CDATA[product development methodologies]]></category>
		<category><![CDATA[product lifecycle management]]></category>
		<category><![CDATA[software embedded products]]></category>
		<category><![CDATA[software innovation]]></category>
		<category><![CDATA[Software tools]]></category>

		<guid isPermaLink="false">http://tech.opensystemsmedia.com/eda/?guid=f338955bd631af06f55a78d839c529bb</guid>
		<description><![CDATA[Software is an opportunity for innovation and differentiation while defining the experience of the end-user.]]></description>
			<content:encoded><![CDATA[<div id='story' class='body'>
<div class='body-text'><img alt="1" class="figure_intro" src="http://i.opensystemsmedia.com/?bg=ffffff&#038;bg=ffffff&#038;fltr[]=over|images/screen2.png|0|0|100&#038;fltr[3]=usm|50|3|0.3&#038;fltr[]=ric|2|2&#038;f=png&#038;h=200&#038;w=225&#038;src=http%3A%2F%2Fattachments.opensystemsmedia.com%2FECD5254%2Ffigures%2F1" /></a>Software is an opportunity for innovation and differentiation &#8212; but also a source of risk that can broadly and deeply affect the success of the entire organization as the software defines the experience of the customers.</p>
<p>This complexity will only continue to grow as an example &#8212; automobiles in the near future, will require 200 to 300 million lines of software code.  To add to the complexity, development of a single product may involve coordinating teams in different locations and time zones.</p>
<p>The only way to achieve this control and collaboration is through the use of a coherent software system lifecycle management solution like Integrity, a PTC product.</p></div>
</p></div>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		</item>
		<item>
		<title>What&#8217;s Hot at DAC 2011</title>
		<link>http://www.youtube.com/watch?v=Y4BCHAIe8yQ&#038;feature=youtube_gdata</link>
		<comments>http://www.youtube.com/watch?v=Y4BCHAIe8yQ&#038;feature=youtube_gdata#comments</comments>
		<pubDate>Mon, 06 Jun 2011 23:17:03 +0000</pubDate>
		<dc:creator>DACPavilion</dc:creator>
				<category><![CDATA[Video]]></category>

		<guid isPermaLink="false">http://gdata.youtube.com/feeds/api/playlists/ED3FCF462DC80CC4/PLFhO0OCIyee_VyYzT_JtvpYicg7bGGBuh</guid>
		<description><![CDATA[Gary Smith of Gary Smith EDA talks about the trends and what's hot at DAC 2011. Gary opens the Pavilion Program on Monday, June 6th at 9:15AM.]]></description>
			<content:encoded><![CDATA[<p>Gary Smith of Gary Smith EDA talks about the trends and what&#8217;s hot at DAC 2011. Gary opens the Pavilion Program on Monday, June 6th at 9:15AM.</p>
]]></content:encoded>
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		<slash:comments>0</slash:comments>
		</item>
		<item>
		<title>Video: Software Design in Medical Devices &#8211; Solving the Quality and Compliance Challenge</title>
		<link>http://www.mil-embedded.com/articles/id/?5156</link>
		<comments>http://www.mil-embedded.com/articles/id/?5156#comments</comments>
		<pubDate>Fri, 15 Apr 2011 15:00:00 +0000</pubDate>
		<dc:creator>Ryan Lloyd, Product Manager, MKS (ALM)</dc:creator>
				<category><![CDATA[Video]]></category>
		<category><![CDATA[alm]]></category>
		<category><![CDATA[application lifecycle management]]></category>
		<category><![CDATA[cmmi process model]]></category>
		<category><![CDATA[compliance]]></category>
		<category><![CDATA[embedded software]]></category>
		<category><![CDATA[iec]]></category>
		<category><![CDATA[iso]]></category>
		<category><![CDATA[iterative software development]]></category>
		<category><![CDATA[lean process improvement]]></category>
		<category><![CDATA[lean sigma process]]></category>
		<category><![CDATA[Medical devices]]></category>
		<category><![CDATA[mks]]></category>
		<category><![CDATA[mks (alm)]]></category>
		<category><![CDATA[product development methodologies]]></category>
		<category><![CDATA[product quality]]></category>
		<category><![CDATA[quality improvement processes]]></category>
		<category><![CDATA[quality management]]></category>
		<category><![CDATA[risk management]]></category>
		<category><![CDATA[Software]]></category>
		<category><![CDATA[software design]]></category>
		<category><![CDATA[software development metrics]]></category>
		<category><![CDATA[software engineering methodology]]></category>
		<category><![CDATA[software life cycle management]]></category>
		<category><![CDATA[software lifecycle model]]></category>
		<category><![CDATA[software lifecycle processes]]></category>
		<category><![CDATA[software qa processes]]></category>
		<category><![CDATA[software quality]]></category>
		<category><![CDATA[systems life cycle management]]></category>
		<category><![CDATA[telehealth]]></category>

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		<description><![CDATA[Medical device engineering teams are looking to improve productivity and quality, streamline compliance, and gain complete product visibility. Watch this video and learn how you can reduce the overwhelming complexity of developing software intensive products and generate compliance reports in mouse clicks instead of weeks.]]></description>
			<content:encoded><![CDATA[<div id='story' class='body'>
<div class='body-text'></a>This video demonstrates how the MKS Integrity solution for Medical Devices, enables engineering organizations to improve software and product quality, automate risk management, efficiently demonstrate compliance and reduce time to market and development costs. With MKS Integrity, engineering teams can:</p>
<p>* Demonstrate compliance in minutes with automated report generation rather than the weeks required with manual processes</p>
<p>* Manage the volume and velocity of software driven change </p>
<p>* Improve team orchestration and reuse design and development artifacts</p>
<p>
</div>
</p></div>
]]></content:encoded>
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