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	<title>GLOBAL REGULATORY AFFAIRS SPOTLIGHTS</title>
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		<title>Harmonized clinical governance regulatory framework for Africa</title>
		<link>http://iraup4all.wordpress.com/2012/02/17/harmonized-clinical-governance-regulatory-framework-for-africa/</link>
		<comments>http://iraup4all.wordpress.com/2012/02/17/harmonized-clinical-governance-regulatory-framework-for-africa/#comments</comments>
		<pubDate>Fri, 17 Feb 2012 06:28:39 +0000</pubDate>
		<dc:creator>globalregulatoryspotlights4all</dc:creator>
				<category><![CDATA[Clinical Trials]]></category>
		<category><![CDATA[Global Health]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[International Regulatory Affairs]]></category>
		<category><![CDATA[Pharmaceuticals]]></category>
		<category><![CDATA[Uncategorized]]></category>
		<category><![CDATA[WHO]]></category>
		<category><![CDATA[African Drug Regulators]]></category>
		<category><![CDATA[Biopharmaceuticals]]></category>
		<category><![CDATA[Ministry of Health]]></category>

		<guid isPermaLink="false">http://iraup4all.wordpress.com/?p=84</guid>
		<description><![CDATA[We need a harmonized clinical governance regulatory framework for Africa. Why or why not? And whose responsibility should it be? Should African governments and private institutions fold their arms and rely on the major pharmaceutical companies in the industrialized world to develop and implement such frameworks for them? My opinion is a “big no, no”. [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=iraup4all.wordpress.com&amp;blog=10126557&amp;post=84&amp;subd=iraup4all&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<title>Steve Jobs&#8217;s Death and e-Clinical Trials</title>
		<link>http://iraup4all.wordpress.com/2011/10/06/steve-jobs-loss-and-e-clinical-trials/</link>
		<comments>http://iraup4all.wordpress.com/2011/10/06/steve-jobs-loss-and-e-clinical-trials/#comments</comments>
		<pubDate>Thu, 06 Oct 2011 05:27:56 +0000</pubDate>
		<dc:creator>globalregulatoryspotlights4all</dc:creator>
				<category><![CDATA[Apple]]></category>
		<category><![CDATA[Clinical Trials]]></category>
		<category><![CDATA[European Medicines Agency]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[Global Health]]></category>
		<category><![CDATA[Global Health Partnership]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[International Regulatory Affairs]]></category>
		<category><![CDATA[Medical Devices]]></category>
		<category><![CDATA[Pharmaceuticals]]></category>
		<category><![CDATA[Steve Jobs]]></category>
		<category><![CDATA[World Health Organization]]></category>
		<category><![CDATA[African Clinical Laboratory]]></category>
		<category><![CDATA[Biopharmaceuticals]]></category>
		<category><![CDATA[Counterfeit drugs]]></category>
		<category><![CDATA[e-Health]]></category>
		<category><![CDATA[Healthy]]></category>
		<category><![CDATA[Ministry of Health]]></category>
		<category><![CDATA[Regulatory Affairs]]></category>

		<guid isPermaLink="false">http://iraup4all.wordpress.com/?p=66</guid>
		<description><![CDATA[FIRST OF ALL,  I WOULD LIKE TO DEDICATE A FEW &#8220;MOMENTS OF SILENCE&#8221; IN MEMORY OF APPLE COMPUTER&#8217;S CO-FOUNDER, STEVE JOBS (1955-2011). In recent years, the impact of Information Technology on Clinical Trials has been profound, to say the least. Smart phones are now gaining momentum in the recruitment of clinical trials volunteers.   Additionally, Smart [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=iraup4all.wordpress.com&amp;blog=10126557&amp;post=66&amp;subd=iraup4all&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<title>The Common Rule Redefined?</title>
		<link>http://iraup4all.wordpress.com/2011/07/26/the-common-rule-redefined/</link>
		<comments>http://iraup4all.wordpress.com/2011/07/26/the-common-rule-redefined/#comments</comments>
		<pubDate>Tue, 26 Jul 2011 04:16:52 +0000</pubDate>
		<dc:creator>globalregulatoryspotlights4all</dc:creator>
				<category><![CDATA[Global Health Partnership]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[International Regulatory Affairs]]></category>
		<category><![CDATA[Medical Devices]]></category>
		<category><![CDATA[Pharmaceuticals]]></category>
		<category><![CDATA[African Clinical Laboratory]]></category>
		<category><![CDATA[African Drug Regulators]]></category>
		<category><![CDATA[Clinical Laboratory Improvements]]></category>
		<category><![CDATA[Clinical Trials]]></category>
		<category><![CDATA[Counterfeit drugs]]></category>
		<category><![CDATA[EMA: European Medicines Agency]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[Ministry of Health]]></category>
		<category><![CDATA[Regulatory Affairs]]></category>
		<category><![CDATA[World Health Organization]]></category>

		<guid isPermaLink="false">http://iraup4all.wordpress.com/?p=28</guid>
		<description><![CDATA[The United States Health And Human Services has, on July 22, 2011, published for public comments, proposed rule changes for protecting human subjects in medical research. This vision has long been overdue in view of the rapid technological, regulatory and scientific advancements taking place globally. Whilst the changes under consideration  focus mostly on the domestic front, [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=iraup4all.wordpress.com&amp;blog=10126557&amp;post=28&amp;subd=iraup4all&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>0</slash:comments>
	
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		<title>Clinical trial improvements in Africa</title>
		<link>http://iraup4all.wordpress.com/2011/07/09/clinical-trial-improvements-in-africa/</link>
		<comments>http://iraup4all.wordpress.com/2011/07/09/clinical-trial-improvements-in-africa/#comments</comments>
		<pubDate>Sat, 09 Jul 2011 06:42:46 +0000</pubDate>
		<dc:creator>globalregulatoryspotlights4all</dc:creator>
				<category><![CDATA[European Medicines Agency]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[International Regulatory Affairs]]></category>
		<category><![CDATA[Pharmaceuticals]]></category>
		<category><![CDATA[World Health Organization]]></category>
		<category><![CDATA[African Drug Regulators]]></category>
		<category><![CDATA[Clinical Laboratory Improvements]]></category>
		<category><![CDATA[Clinical Trials]]></category>
		<category><![CDATA[Counterfeit drugs]]></category>
		<category><![CDATA[EMA: European Medicines Agency]]></category>
		<category><![CDATA[Ministry of Health]]></category>
		<category><![CDATA[Regulatory Affairs]]></category>

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		<description><![CDATA[With the rising cost of new healthcare products development in the industrialized world, the developing countries of Africa, where the cost of labor is comparatively cheap, are becoming a hub for clinical testing of drugs and medical devices. The problem, though, is that most of these countries do not have their own national regulations governing [...]<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=iraup4all.wordpress.com&amp;blog=10126557&amp;post=15&amp;subd=iraup4all&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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		<slash:comments>0</slash:comments>
	
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		<title>Clinical Trials in Africa</title>
		<link>http://iraup4all.wordpress.com/2009/10/26/clinical-trials-in-africa/</link>
		<comments>http://iraup4all.wordpress.com/2009/10/26/clinical-trials-in-africa/#comments</comments>
		<pubDate>Mon, 26 Oct 2009 22:58:21 +0000</pubDate>
		<dc:creator>globalregulatoryspotlights4all</dc:creator>
				<category><![CDATA[CLIA]]></category>
		<category><![CDATA[Global Health Partnership]]></category>
		<category><![CDATA[health]]></category>
		<category><![CDATA[WHO]]></category>
		<category><![CDATA[African Drug Regulators]]></category>
		<category><![CDATA[CLIA Regulations]]></category>
		<category><![CDATA[Clinical Laboratory Improvements]]></category>
		<category><![CDATA[Clinical Laboratory Licensure in Africa]]></category>
		<category><![CDATA[Clinical Trials]]></category>
		<category><![CDATA[Counterfeit drugs]]></category>
		<category><![CDATA[EMA: European Medicines Agency]]></category>
		<category><![CDATA[FDA]]></category>
		<category><![CDATA[Medical Devices]]></category>
		<category><![CDATA[Ministry of Health]]></category>
		<category><![CDATA[Regulatory Affairs]]></category>
		<category><![CDATA[World Health Organization]]></category>

		<guid isPermaLink="false">http://iraup4all.wordpress.com/?p=3</guid>
		<description><![CDATA[Whilst medical products clinical trials in Africa is becoming the &#8220;new African gold&#8221;, a number of topics need to be addressed including, but not limited to, language requirements, volunteer compensation, ethical treatment of subjects and infrastructure. What roles are the African Union (AU), private sector personnel and National Governments playing to make these &#8220;new gold deposits&#8221; sustainable?<img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=iraup4all.wordpress.com&amp;blog=10126557&amp;post=3&amp;subd=iraup4all&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
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