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	<title>GCP Helpdesk Webinars</title>
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		<title>GCP Helpdesk Webinars</title>
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		<title>Webinar on GCP in China/Korea/India – Commonalities/Differences &#8211; 9th December 2011</title>
		<link>http://gcphelpdeskevents.wordpress.com/2011/11/29/gcp-chaina-korea-india/</link>
		<comments>http://gcphelpdeskevents.wordpress.com/2011/11/29/gcp-chaina-korea-india/#comments</comments>
		<pubDate>Tue, 29 Nov 2011 06:30:28 +0000</pubDate>
		<dc:creator>gcphelpdeskevents</dc:creator>
				<category><![CDATA[Clinical Trials]]></category>
		<category><![CDATA[Clinical Trial Guidelines]]></category>
		<category><![CDATA[Gcp]]></category>
		<category><![CDATA[Gcp Clinical Research]]></category>
		<category><![CDATA[Good Clinical Practice Guidance]]></category>
		<category><![CDATA[Good Clinical Practice Guidelines]]></category>
		<category><![CDATA[Good Clinical Practice Regulations]]></category>

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		<description><![CDATA[As the establishment of environment for clinical trials in Asia is sound, the efforts like harmonization of GCP, Special trainings, reviews, consultation of clinical trials has been started to provide ethnic concerns in accepting other country clinical data. GCPHelpdesk.com is &#8230; <a href="http://gcphelpdeskevents.wordpress.com/2011/11/29/gcp-chaina-korea-india/">Continue reading <span class="meta-nav">&#8594;</span></a><img alt="" border="0" src="http://stats.wordpress.com/b.gif?host=gcphelpdeskevents.wordpress.com&amp;blog=29935599&amp;post=4&amp;subd=gcphelpdeskevents&amp;ref=&amp;feed=1" width="1" height="1" />]]></description>
			<content:encoded><![CDATA[<p>As the establishment of environment for clinical trials in Asia is sound, the efforts like harmonization of GCP, Special trainings, reviews, consultation of clinical trials has been started to provide ethnic concerns in accepting other country clinical data.</p>
<p>GCPHelpdesk.com is honored to organize a webinar on “<strong>GCP in China/Korea/India – Commonalities/Differences</strong>” in a plan to assist all the CRAs, Project Managers, Regulatory teams, CRCs, and Quality Assurance in improving their exposure and their understanding of the GCP in different countries.</p>
<p><strong>Key Topic Of Webinar</strong>:Implementing GCP in China/Korea/India</p>
<p><strong>Who should participate?</strong></p>
<p>• Clinical Operations<br />
• Project Management<br />
• Monitors<br />
• Investigators<br />
• QA<br />
• Regulatory and all other clinical professionals</p>
<div><strong><span style="font-family:Verdana;font-size:12px;">Speakers</span></strong></div>
<div><img src="http://www.makrocare.com/Images/articles/yang.jpg" alt="" width="75" height="75" border="0" /></div>
<p><span style="font-family:Verdana;font-size:12px;"><strong>Dr. David Yang</strong><br />
Co-founder and CEO of MicroConstants, China</span></p>
<div><img src="http://www.makrocare.com/Images/articles/Rahul.jpg" alt="" width="75" height="75" border="0" /></div>
<p><span style="font-family:Verdana;font-size:12px;"><strong>Mr. Rahul Gowda</strong><br />
Manager- Project Management for Global Clinical Trials, LSK Global Pharma, South Korea</span></p>
<div><strong class="blue_B"><span style="font-family:Verdana;font-size:12px;">Facilitator </span></strong></div>
<div><img src="http://www.makrocare.com/Images/articles/laxman.jpg" alt="" width="75" height="75" border="0" /></div>
<p><span style="font-family:Verdana;font-size:12px;"><strong>Laxman Jakkala, Ph.D</strong><br />
Global Clinical-QA, GCP Helpdesk </span></p>
<p><strong>Date</strong> : Friday, 9th December 2011<br />
<strong>Timings:</strong><br />
5:30 PM to 7:00 PM (Singapore)<br />
6:30 PM to 8:00 PM (KST/JST)<br />
3:00 PM to 4:30 PM (IST)<br />
10:30 AM to 12:00 PM (CET)<br />
<strong>Webinar:</strong> From your own Desk (Internet connection and head set / speakers)<br />
<strong>Cost:</strong> None</p>
<p><strong><a title="GCP-Chaina-Korea-India" href="http://www.gcphelpdesk.com/index.php/gcp-webinar">Click Here</a></strong> for more information about this webinar<br />
<strong>How to Register: <a title="Clinical Trial Guidelines" href="http://www.makrocare.com/index.php/webinargcp">Click here and confirm your presence now</a></strong> or Send your information for registration to <strong><a href="mailto:webinar@gcphelpdesk.com">webinar@gcphelpdesk.com</a></strong></p>
<div><a title="Clinical Research India" href="http://www.makrocare.com/"><img class="alignleft" style="border:0 none;" title="Clinical Trial Guidelines" src="http://www.makrocare.com/Images/articles/Makrocare_logo.jpg" alt="Clinical Research India" width="75" height="75" border="0" /></a></div>
<p><span style="font-family:Verdana;font-size:12px;"><strong></strong>MakroCare, an international drug development and commercialization partner that is dedicated to efficient, high-level performance in combination with unparalleled client satisfaction. MakroCare has 5 subsidiaries/divisions – CRO, SMO, Consulting, DDi and Commercialization. MakroCare has teams positioned worldwide in these divisions supporting regulatory affairs, risk management, trial management (clinical, late phase), monitoring, biometrics (CDM, EDC, Biostatistics, SAS programming, medical writing), QA audits, drug safety / PV, site management, patient recruitment/retention, informatics (EDC, CTMS, IVRS), marketing/sales, branding, and contact center.</span></p>
<div><a title="Clinical Research Trials" href="http://www.gcphelpdesk.com/"><img class="alignleft" style="border:0 none;" title="Clinical Research Trials" src="http://www.makrocare.com/Images/articles/GCP_logo.jpg" alt="GCP HelpDesk" width="75" height="75" border="0" /></a></div>
<p><span style="font-family:Verdana;font-size:12px;"><strong></strong>MakroCare&#8217;s objective to launch GCPHelpdesk- a non profitable website is to help the clinical research professionals to understand the questions regarding clinical trial conducting and managing clinical research as per GCP,DCGI, SFDA (China), US FDA, HSA, EMA and other applicable Regulations. This is aimed to provide transparency from resources and expertise in the field of Clinical Research with the recent developments and changes in the guidelines for clinical research professionals.</span></p>
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