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	<description>Global Research Partner</description>
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		<title>Technology Partners</title>
		<link>https://aqlivia.com/technology-partners/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Thu, 25 Apr 2019 03:15:22 +0000</pubDate>
				<category><![CDATA[Aqlivia]]></category>
		<guid isPermaLink="false">https://aqlivia.com/?p=1192</guid>

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		<title>Global Foot Print</title>
		<link>https://aqlivia.com/global-foot-print/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Thu, 25 Apr 2019 03:15:07 +0000</pubDate>
				<category><![CDATA[Aqlivia]]></category>
		<guid isPermaLink="false">https://aqlivia.com/?p=1190</guid>

					<description><![CDATA[India APAC Head Quarter, # 005, The Mark Structure, Unique Infra Building, Next to Tennis court, North Bangalore – 560097 &#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195; European Head Quarter, Vishnuplantsoen 9, 1363XD ALMERE, Netherlands, Phone number: +31 6 1562 4933 &#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195;&#8195; Regional office Japan, Kyoto Research Park, Unique Kyoto City, Kyoto – 6008813 India Netherlands Australia United-Kingdom Japan]]></description>
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<font face = "Helvetica" size = "5">India APAC Head Quarter, # 005, The Mark Structure, Unique Infra Building, Next to Tennis court, North Bangalore – 560097

&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;

<font face = "Helvetica" size = "5">European Head Quarter, Vishnuplantsoen 9, 1363XD ALMERE, Netherlands, Phone number: +31 6 1562 4933

&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;&emsp;

<font face = "Helvetica" size = "5">Regional office Japan, Kyoto Research Park, Unique Kyoto City, Kyoto – 6008813
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										<img decoding="async" src="https://aqlivia.com/wp-content/uploads/elementor/thumbs/flag-of-India-om6i9t3u9bpw7u447c9wyz3c06303lixptx6m643w4.png" title="flag-of-India" alt="India" loading="lazy" />											<figcaption class="widget-image-caption wp-caption-text">India</figcaption>
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		<title>Sites</title>
		<link>https://aqlivia.com/sites/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Thu, 25 Apr 2019 03:14:46 +0000</pubDate>
				<category><![CDATA[Aqlivia]]></category>
		<guid isPermaLink="false">https://aqlivia.com/?p=1188</guid>

					<description><![CDATA[]]></description>
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		<title>RADIO IMAGING TRAILS</title>
		<link>https://aqlivia.com/radio-imaging-trails/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Tue, 23 Apr 2019 09:20:02 +0000</pubDate>
				<category><![CDATA[Aqlivia]]></category>
		<guid isPermaLink="false">https://aqlivia.com/?p=1154</guid>

					<description><![CDATA[Radio Imaging Trails Drug development continues to face challenges to successfully progress the most promising drug candidates through the stages of clinical trials. Given the increasing cost to develop a drug, methods are required to characterize early drug efficacy and safety. Imaging techniques are increasingly used in oncological clinical trials to provide evidence for decision [&#8230;]]]></description>
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									<h6><span style="color: #000000;">Drug development continues to face challenges to successfully progress the most promising drug candidates through the stages of clinical trials. Given the increasing cost to develop a drug, methods are required to characterize early drug efficacy and safety. Imaging techniques are increasingly used in oncological clinical trials to provide evidence for decision making. With the application of conventional morphological imaging techniques and standardized response criteria based on tumour size measurements, imaging continues to be used to define key study end points. However, functional imaging techniques are likely to play an important role in the evaluation of novel therapeutics, although how these methods are to be optimally applied has yet to be clearly established. The specific challenges of standardising multi-centre imaging in the context of clinical trials are highlighted, including the processes for image acquisition, data analysis and radiological review.</span></h6><h6><span style="color: #000000;">AQLIVIA Informatics is a global leader in helping pharmaceutical and biotech companies employ time- and budget-saving medical imaging in clinical trials.</span></h6><h6><span style="color: #000000;">Our expertise spans a wide-range of therapeutic areas including Oncology, Musculoskeletal, Neurology, Cardiovascular, Women&#8217;s Health, Gastroenterology, Ophthalmology, Dermatology and Volumetric. AQLIVIA Informatics’ full range of services comprises all necessary pieces for successful trial imaging implementation including:</span></h6><h6><strong><span style="color: #000000;">Our Medical Imaging experts also provide:</span></strong><br /><span style="color: #000000;">• Protocol and study design consultation</span><br /><span style="color: #000000;">• Site training</span><br /><span style="color: #000000;">• Perceptive MyTrials Medical Imaging technology suite to simplify processes for sites</span><br /><span style="color: #000000;">• Image collection and QC</span><br /><span style="color: #000000;">• Independent Review Charter development and support with SPA submissions</span><br /><span style="color: #000000;">• Centralized independent review and reader management services</span><br /><span style="color: #000000;">• Full data reconciliation and export</span><br /><span style="color: #000000;">• Regulatory filing and submission support</span><br /><span style="color: #000000;">• Image archiving and sharing</span></h6>								</div>
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		<title>MEDICAL DEVICE TRAILS</title>
		<link>https://aqlivia.com/medical-device-trails/</link>
		
		<dc:creator><![CDATA[admin]]></dc:creator>
		<pubDate>Tue, 23 Apr 2019 06:41:02 +0000</pubDate>
				<category><![CDATA[Aqlivia]]></category>
		<guid isPermaLink="false">https://aqlivia.com/?p=1145</guid>

					<description><![CDATA[Medical Device Trails Compliance with the Medical Device Directive, and in the near future the Medical Device Regulation, is vital to be able to obtain and/or maintain CE-marking. Performing a clinical study is a serious and costly undertaking for every medical device manufacturer, requiring a strategic and practical approach. Aqlivia has years of experience in [&#8230;]]]></description>
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									<h6><span style="color: #000000;">Compliance with the Medical Device Directive, and in the near future the Medical Device Regulation, is vital to be able to obtain and/or maintain CE-marking. Performing a clinical study is a serious and costly undertaking for every medical device manufacturer, requiring a strategic and practical approach.</span></h6><h6><span style="color: #000000;">Aqlivia has years of experience in regulatory affairs. Aqlivia CRO offers you the same, high level of expertise in clinical affairs. We support all kinds of trials for Class I Class III medical devices, to help you collect high quality, ISO14155, compliant clinical data. Our services include Clinical Strategy, Study start up, Monitoring, Data Management, Auditing, Training, Medical Writing, EC/CA/IRB communication, Project Management.</span></h6><p><span style="color: #000000;">We truly believe in a strategic, notified body proof and overall practical approach. Setting-up clinical trials tailored to your medical device specific needs.</span><br /><span style="color: #000000;">Aqlivia dedicated and experienced in all kinds of indications including urology, neurology, dental, cardiovascular, orthopedics, ophthalmology, imaging, etc. Our clinical team gained experience working at Notified Bodies, CRO’s and Sponsors/Manufacturers. This combination of different backgrounds, combined with Aqlivia’s in-depth knowledge of regulatory affair creates efficient and compliant clinical trials. Our expertise includes feasibility, pre-CE and post-market studies from class I to class III. </span><br /><span style="color: #000000;">Because of our regulatory expertise, we are able to provide our practical approach, leading to tailored trials. </span></p>								</div>
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