http://ctwc.work/ctwc/index.php/campaigns/mg879emt9ma73/track-url/hr930t4rro205/a23fe9f7b8ea6d7599b90b8cc3b0def4de120150

Last Checked: May 15, 2019, 17:27 EDT

IP Address: 77.104.143.211
ASN #: AS36351 SOFTLAYER - SoftLayer Technologies Inc., US
Location: Data unavailable.
URL Reputation:
  • Unknown This URL is not identified as malicious in the PhishTank Database.
  • Unknown PhishCheck thinks this URL is likely not a phish.
  • Unknown OpenPhish: URL not in feed.

Other submissions on 77.104.143.211:

  • http://ctwc.online/ctwc/index.php/campaigns/wt071slbf9ffa/track-url/la4424w9m5d0a/5687c5843c27a6de7afdd93a7ad96dd6cd5b5cb2

  • http://ctwc.online/ctwc/index.php/campaigns

  • http://ctwc.online/ctwc/index.php/campaigns/tt68324142d6d/track-url/vx553dbmhd3f6/1d1526902c9b1946c750085da129ee4ae07c0aa3

  • http://ctwc.online/ctwc/index.php/campaigns/je649nevhqb59/track-url/hl176zlvqf52b/3a07cd4d37714573ba1f17c21ee56b3a35a6478f

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  • http://ctwc.work/ctwc/index.php/campaigns/qs929mh0bk7e2/report-abuse/zv046n3xvm603/wg2721xpz596a

  • http://ctwc.work/ctwc/index.php/campaigns/mg879emt9ma73/track-url/hr930t4rro205/2e3dfc735cd7fae11590306622158e81f1bed1e6

  • http://ctwc.work/

  • http://ctwc.online/ctwc/index.php/campaigns/yq008b9d0214e/track-opening/rb3021yr7gb6d

Other submissions on ctwc.work:

  • http://ctwc.work/ctwc/index.php/campaigns/mg879emt9ma73/track-url/hr930t4rro205/2e3dfc735cd7fae11590306622158e81f1bed1e6

  • http://ctwc.work/

  • http://ctwc.work/ctwc/index.php/campaigns/mg879emt9ma73/track-opening/hr930t4rro205

  • http://ctwc.work/ctwc/index.php/lists/zv046n3xvm603/unsubscribe/wg2721xpz596a/qs929mh0bk7e2/unsubscribe-direct?source=email-client-unsubscribe-button

  • http://ctwc.work/ctwc/index.php/lists/block-address

  • http://ctwc.work/ctwc/index.php/campaigns/qs929mh0bk7e2/report-abuse/zv046n3xvm603/wg2721xpz596a

Previous checks:

                               Domain Name: CTWC.WORK
Registry Domain ID: D_00E61D84_FE1F9F5142E74A4CAAB2CD84EB58C08F_00000169B9F9E916-WORK
Registrar WHOIS Server: 
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Updated Date: 2019-04-03T16:26:14Z
Creation Date: 2019-03-26T12:29:16Z
Registry Expiry Date: 2020-03-26T12:29:16Z
Registrar: GoDaddy.com, LLC
Registrar IANA ID: 146
Registrar Abuse Contact Email: abuse@godaddy.com
Registrar Abuse Contact Phone: +1.4806242505
Domain Status: clientDeleteProhibited https://icann.org/epp#clientDeleteProhibited
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Billing Email: Please query the RDDS service of the Registrar of Record identified in this output for information on how to contact the Registrant, Admin, or Tech contact of the queried domain name.
Name Server: ns1.c62408.sgvps.net.
Name Server: ns2.c62408.sgvps.net.
DNSSEC: unsigned
URL of the ICANN Whois Inaccuracy Complaint Form: https://www.icann.org/wicf/
>>> Last update of WHOIS database: 2019-05-15T21:27:16Z <<<

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  • 301 Moved Permanently

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

    GET HTTP/2.0 https://webinarcompliance.com/wp-includes/js/jquery/jquery-migrate.min.js?ver=1.4.1

  • 200

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  • 200

    GET HTTP/2.0 https://webinarcompliance.com/wp-includes/js/jquery/jquery.js?ver=1.12.4

  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • 200

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  • http://ctwc.work/ctwc/index.php/campaigns/mg879emt9ma73/track-url/hr930t4rro205/a23fe9f7b8ea6d7599b90b8cc3b0def4de120150 https://webinarcompliance.com/product/building-qbd-and-rbqm-systems-into-clinical-operations-marina-malikova-fdb2837/?utm_source=mailwizzd1&utm_medium=email&utm_campaign=building-qbd-and-rbqm
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<div itemscope="" itemtype="http://schema.org/Product" id="product-23123" class="post-23123 product type-product status-publish has-post-thumbnail webinar-types-live-webinar webinar-types-on-demand-webinar product_cat-clinical-laboratory product_cat-food-drugs-biologics product_cat-asq product_tag-qbd product_tag-rbqm first instock shipping-taxable purchasable product-type-variable has-default-attributes has-children">

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				<h1 class="page-title">Building QbD and RBQM Systems into Clinical Operations </h1>
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			<li>Product Id : FDB2837</li>
			<li>Category :     <a href="https://webinarcompliance.com/product-category/clinical-laboratory/" rel="tag">Clinical &amp; Laboratory</a>, <a href="https://webinarcompliance.com/product-category/food-drugs-biologics/" rel="tag">Food, Drugs &amp; Biologics</a>, <a href="https://webinarcompliance.com/product-category/asq/" rel="tag">Quality</a> </li>
			<li>Presenter : <a href="https://webinarcompliance.com/author/dr-marina-malikova/" rel="author">Marina Malikova</a></li>
						<li>Duration : 90 Minutes</li>
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<p>This session is focused on Quality by Design (QbD) and new regulatory requirements for Risk-Based monitoring and building Risk-Based Quality Management (RBQM) systems.</p>
<p>Besides being a new expectation by regulatory agencies under good clinical practices, Quality by Design (QbD) and Risk-Based Quality Management (RBQM) concepts are receiving attention on a world-wide basis. As the industry’s utilization of risk-based monitoring continues to increase along with the development and expansion of the area of RBQM, the need for the integration of these two concepts becomes apparent.</p>
<p>The premise behind RBQM is that monitoring quality can be improved by leveraging existing data intelligence. This, in turn, calls for more robust quality assurance (QA) systems focused and efficient resource utilization and allocation at the clinical site, CROs and Sponsors level.</p>
<p><span style="color: #1b88d6;"><strong>Why You Should Attend:</strong></span></p>
<p>RBQM is the proactive identification and mitigation of risks. By combining these two concepts, the inherent risks identified up front can feed into the design of the risk-based monitoring plan QbD. RBQM requires development of well-defined and relevant metrics, key performance and quality indicators (KP-QI), as well as a solid process for review and follow-up of the identified signals. Both aspects need to be supported by robust information management as well as training and cross-functional communication strategies.</p>
<p>Practical aspects of developing key performance and quality indicators at all stages of clinical trials will be discussed. Building Quality Management Systems for Sites and Sponsors: Cause-Effect Analysis and Corrective Action Preventive Action (CAPA) plans will be also available as a workshop as part of this course providing an interactive exploration of quality management systems and preparing you to build them in both site and sponsor settings to improve clinical trial operations efficiency and accuracy.</p>
<div style="float: left; width: 50%;">
<span style="color: #1b88d6;"><strong>Areas Covered in the Session :</strong></span><p></p>
<ul>
<li>Describe principles of Quality by Design (QbD) and new regulatory requirement for Risk-based monitoring</li>
<li>Develop relevant metrics as quality and performance indicators for Risk-Based Quality Management (RBQM) systems</li>
<li>Identify and manage risks of clinical trials</li>
<li>Perform Cause-Effect Analysis for identified risks and develop mitigation strategy</li>
<li>Review recent noncompliance trends and regulatory focus for Sites, Sponsors, and IRBs</li>
<li>Develop effective Corrective Action Preventive Action (CAPA) Plans</li>
</ul>
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<span style="color: #1b88d6;"><strong>Who Should Attend:</strong></span><p></p>
<ul>
<li>Clinical Quality Assurance Auditors </li>
<li>Clinical Quality and Compliance Professionals </li>
<li>Clinical Research Associates </li>
<li>Project Managers </li>
<li>Medical Monitors </li>
<li>Regulatory Affairs Professionals </li>
<li>Clinical Research Coordinators </li>
<li>Clinical Principal Investigators </li>
<li>IRB Administrators and Members</li>
</ul>
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<p><font style="font-size:0px">FDB2837</font></p>
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			<h4>Marina Malikova</h4>
			<p>Dr. Malikova has over twenty years of experience in the clinical research field. She has managed Phase I – IV studies involving investigational drugs, devices and biologics. She has worked on Industry-sponsored and Investigator-initiated trials in the fields of Surgery, Cancer Diagnostics and Interventional Radiology.</p>
<p>Dr. Malikova graduated from the Institute of Biochemistry, Russian Academy of Science, in Moscow, Russia with a PhD in Biochemistry. She also holds a Master’s Degree in Clinical Investigation and Project Management Certification from Boston University.</p>
<p>In her current role as Executive Director, Dr. Malikova manages research efforts in 13 divisions of the Department of Surgery at Boston Medical Center. She is responsible for clinical trials and basic biomedical research operations, quality assurance, risk management, safety monitoring, strategic planning, and macro-management of research programs. She provides guidance and oversight to the Project Managers, Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), and laboratory staff. She advises faculty/staff on protocol and informed consent writing; assists with BU IRB applications and submissions; provides oversight for data user agreements, cost coverage analysis and budgets development, contracts and licensing for clinical research; and ensures compliance.</p>
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		<p>Webinar Compliance reserves the right to cancel or reschedule any Webinar/event due to inevitable reasons such as insufficient registrations or circumstances beyond its control. All the attendees will be notified about the cancellation of the event, 24 hours prior to the start time of the Webinar event.</p>

<p>The cancelled Webinar, could be rescheduled and a New Date would be promptly intimated to the attendees.</p>

<p><strong>In such an event, the attendee can opt for one of the below :</strong></p>

<ol>
<li>If the New Date is not of convenience, the webinar stream (1-Time Recording) may be availed.</li>
<li>The attendees may also opt to take a different webinar, which has a same price tag at a future date &amp; time; they are welcome to do so.</li>
<li>On-Demand recordings (Past events) in exchange but equal to the original amount remitted.</li>
<li>A redeemable voucher (Valid for 12 months), which could be used to purchase any of our future events.</li>
<li>Webinar Compliance will process refund only if an event that has been cancelled, is not rescheduled within 90 days from the original scheduled date of the webinar.
</li><li>If a webinar is canceled completely, an attendee may opt either of above points 2,3,4, or a full refund of the amount paid in a single settlement. The payment will be processed within 7 Business days from the day, we receive the refund request. However, Webinar Compliance will not be responsible for any penalties or other expenditure incurred due to the cancellation.</li>
</ol>

<p>​Individual attendees can cancel their event for any specific reason. They must notify Webinar Compliance about the cancellation of their registration at least 48 hours prior to the event start date and time.</p>

<p>If the attendee fails to cancel the registration to the event within the above mentioned stipulated time or if fails to attend the event, no refund shall be made.</p>

​<p>​For further clarification on the refund or cancellation policy, you can contact the support team over the phone or please write to us on <a href="mailto:support@webinarcompliance.com">support@webinarcompliance.com</a>, with the transaction ID, event ID &amp; event date in the subject column.</p>	</div>
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