ºÝºÝߣshows by User: DATATRAK / http://www.slideshare.net/images/logo.gif ºÝºÝߣshows by User: DATATRAK / Fri, 08 May 2015 15:35:23 GMT ºÝºÝߣShare feed for ºÝºÝߣshows by User: DATATRAK eSource: Data Capture Simplified - Uncover Time and Cost Saving Possibilities /slideshow/cbi-e-source-presentation-bill-gluck-final/47916431 cbiesourcepresentationbillgluckfinal-150508153523-lva1-app6892
In this presentation, Dr. Gluck discusses streamlining data capture in clinical trials uncovering time and cost savings possibilities.]]>

In this presentation, Dr. Gluck discusses streamlining data capture in clinical trials uncovering time and cost savings possibilities.]]>
Fri, 08 May 2015 15:35:23 GMT /slideshow/cbi-e-source-presentation-bill-gluck-final/47916431 DATATRAK@slideshare.net(DATATRAK) eSource: Data Capture Simplified - Uncover Time and Cost Saving Possibilities DATATRAK In this presentation, Dr. Gluck discusses streamlining data capture in clinical trials uncovering time and cost savings possibilities. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/cbiesourcepresentationbillgluckfinal-150508153523-lva1-app6892-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> In this presentation, Dr. Gluck discusses streamlining data capture in clinical trials uncovering time and cost savings possibilities.
eSource: Data Capture Simplified - Uncover Time and Cost Saving Possibilities from www.datatrak.com
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Leverage Your EDC Solution to Mitigate Risk in Clinical Research /slideshow/leverage-your-edc-solution-to-mitigate-risk-in-clinical-research-46286041/46286041 mitigateriskwebinar-3-25-2015-150325150016-conversion-gate01
Every clinical trial is built upon a study protocol - the cornerstone of any trial. A well-defined and written study protocol provides the blueprint for the study, defining its purpose and goals. Studies have become more complex, creating more complicated study design, which can lead to making adherence more challenging for the study team and participants. The potential risk that some aspect of the study could be done incorrectly or not comply is inherent in all studies, but particularly present in complex research. In order to help mitigate risk, advances in technology and the tools available today provide ways for us to mitigate some of the risk introduced in our clinical trials. While the study protocol is a cornerstone for the clinical trial, electronic data capture (EDC) applications have evolved in the broadest sense into technology solutions that provide us with a variety of tools to help mitigate risk.]]>

Every clinical trial is built upon a study protocol - the cornerstone of any trial. A well-defined and written study protocol provides the blueprint for the study, defining its purpose and goals. Studies have become more complex, creating more complicated study design, which can lead to making adherence more challenging for the study team and participants. The potential risk that some aspect of the study could be done incorrectly or not comply is inherent in all studies, but particularly present in complex research. In order to help mitigate risk, advances in technology and the tools available today provide ways for us to mitigate some of the risk introduced in our clinical trials. While the study protocol is a cornerstone for the clinical trial, electronic data capture (EDC) applications have evolved in the broadest sense into technology solutions that provide us with a variety of tools to help mitigate risk.]]>
Wed, 25 Mar 2015 15:00:16 GMT /slideshow/leverage-your-edc-solution-to-mitigate-risk-in-clinical-research-46286041/46286041 DATATRAK@slideshare.net(DATATRAK) Leverage Your EDC Solution to Mitigate Risk in Clinical Research DATATRAK Every clinical trial is built upon a study protocol - the cornerstone of any trial. A well-defined and written study protocol provides the blueprint for the study, defining its purpose and goals. Studies have become more complex, creating more complicated study design, which can lead to making adherence more challenging for the study team and participants. The potential risk that some aspect of the study could be done incorrectly or not comply is inherent in all studies, but particularly present in complex research. In order to help mitigate risk, advances in technology and the tools available today provide ways for us to mitigate some of the risk introduced in our clinical trials. While the study protocol is a cornerstone for the clinical trial, electronic data capture (EDC) applications have evolved in the broadest sense into technology solutions that provide us with a variety of tools to help mitigate risk. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/mitigateriskwebinar-3-25-2015-150325150016-conversion-gate01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Every clinical trial is built upon a study protocol - the cornerstone of any trial. A well-defined and written study protocol provides the blueprint for the study, defining its purpose and goals. Studies have become more complex, creating more complicated study design, which can lead to making adherence more challenging for the study team and participants. The potential risk that some aspect of the study could be done incorrectly or not comply is inherent in all studies, but particularly present in complex research. In order to help mitigate risk, advances in technology and the tools available today provide ways for us to mitigate some of the risk introduced in our clinical trials. While the study protocol is a cornerstone for the clinical trial, electronic data capture (EDC) applications have evolved in the broadest sense into technology solutions that provide us with a variety of tools to help mitigate risk.
Leverage Your EDC Solution to Mitigate Risk in Clinical Research from www.datatrak.com
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Defining a Central Monitoring Capability: Sharing the Experience of TransCelerate BioPharma's Approach Part I /slideshow/therapeutic-innovation-regulatory-science-2014wilson52935definingcentralmonitoringcapability/40601926 therapeuticinnovationregulatoryscience-2014-wilson-529-35-defining-central-monitoring-capability-141022114912-conversion-gate01
Central monitoring, on-site monitoring, and off-site monitoring provide an integrated approach to clinical trial quality management. TransCelerate distinguishes central monitoring from other types of central data review activities and puts it in the context of an overall monitoring strategy. Any organization seeking to implement central monitoring will need people with the right skills, technology options that support a holistic review of study-related information, and adaptable processes. There are different approaches actively being used to implement central monitoring. This article provides a description of how companies are deploying central monitoring, as well as samples of the workflows that illustrate how some have implemented it. The desired outcomes include earlier, more predictive detection of quality issues. This paper describes the initial implementation steps designed to learn what organizational capabilities are necessary.]]>

Central monitoring, on-site monitoring, and off-site monitoring provide an integrated approach to clinical trial quality management. TransCelerate distinguishes central monitoring from other types of central data review activities and puts it in the context of an overall monitoring strategy. Any organization seeking to implement central monitoring will need people with the right skills, technology options that support a holistic review of study-related information, and adaptable processes. There are different approaches actively being used to implement central monitoring. This article provides a description of how companies are deploying central monitoring, as well as samples of the workflows that illustrate how some have implemented it. The desired outcomes include earlier, more predictive detection of quality issues. This paper describes the initial implementation steps designed to learn what organizational capabilities are necessary.]]>
Wed, 22 Oct 2014 11:49:12 GMT /slideshow/therapeutic-innovation-regulatory-science-2014wilson52935definingcentralmonitoringcapability/40601926 DATATRAK@slideshare.net(DATATRAK) Defining a Central Monitoring Capability: Sharing the Experience of TransCelerate BioPharma's Approach Part I DATATRAK Central monitoring, on-site monitoring, and off-site monitoring provide an integrated approach to clinical trial quality management. TransCelerate distinguishes central monitoring from other types of central data review activities and puts it in the context of an overall monitoring strategy. Any organization seeking to implement central monitoring will need people with the right skills, technology options that support a holistic review of study-related information, and adaptable processes. There are different approaches actively being used to implement central monitoring. This article provides a description of how companies are deploying central monitoring, as well as samples of the workflows that illustrate how some have implemented it. The desired outcomes include earlier, more predictive detection of quality issues. This paper describes the initial implementation steps designed to learn what organizational capabilities are necessary. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/therapeuticinnovationregulatoryscience-2014-wilson-529-35-defining-central-monitoring-capability-141022114912-conversion-gate01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Central monitoring, on-site monitoring, and off-site monitoring provide an integrated approach to clinical trial quality management. TransCelerate distinguishes central monitoring from other types of central data review activities and puts it in the context of an overall monitoring strategy. Any organization seeking to implement central monitoring will need people with the right skills, technology options that support a holistic review of study-related information, and adaptable processes. There are different approaches actively being used to implement central monitoring. This article provides a description of how companies are deploying central monitoring, as well as samples of the workflows that illustrate how some have implemented it. The desired outcomes include earlier, more predictive detection of quality issues. This paper describes the initial implementation steps designed to learn what organizational capabilities are necessary.
Defining a Central Monitoring Capability: Sharing the Experience of TransCelerate BioPharma's Approach Part I from www.datatrak.com
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Technology Considerations to Enable the Risk-Based Monitoring Methodology /slideshow/therapeutic-innovation-regulatory-science-2014barnes53645technologyconsiderations/40601425 therapeuticinnovationregulatoryscience-2014-barnes-536-45-technology-considerations-141022113727-conversion-gate01
TransCelerate BioPharma Inc developed a methodology based on the notion that shifting monitoring processes from an excessive concentration on source data verification to comprehensive risk-driven monitoring will increase efficiencies and enhance patient safety and data integrity while maintaining adherence to good clinical practice regulations. This philosophical shift in monitoring processes employs the addition of centralized and off-site mechanisms to monitor important trial parameters holistically, and it uses adaptive on-site monitoring to further support site processes, subject safety, and data quality. The main tenet is to use available data to monitor, assess, and mitigate the overall risk associated with clinical trials. Having the right technology is critical to collect and aggregate data, provide analytical capabilities, and track issues to demonstrate that a thorough quality management framework is in place. This paper lays out the high-level considerations when designing and building an integrated technology solution that will aid in scaling the methodology across an organization’s portfolio.]]>

TransCelerate BioPharma Inc developed a methodology based on the notion that shifting monitoring processes from an excessive concentration on source data verification to comprehensive risk-driven monitoring will increase efficiencies and enhance patient safety and data integrity while maintaining adherence to good clinical practice regulations. This philosophical shift in monitoring processes employs the addition of centralized and off-site mechanisms to monitor important trial parameters holistically, and it uses adaptive on-site monitoring to further support site processes, subject safety, and data quality. The main tenet is to use available data to monitor, assess, and mitigate the overall risk associated with clinical trials. Having the right technology is critical to collect and aggregate data, provide analytical capabilities, and track issues to demonstrate that a thorough quality management framework is in place. This paper lays out the high-level considerations when designing and building an integrated technology solution that will aid in scaling the methodology across an organization’s portfolio.]]>
Wed, 22 Oct 2014 11:37:27 GMT /slideshow/therapeutic-innovation-regulatory-science-2014barnes53645technologyconsiderations/40601425 DATATRAK@slideshare.net(DATATRAK) Technology Considerations to Enable the Risk-Based Monitoring Methodology DATATRAK TransCelerate BioPharma Inc developed a methodology based on the notion that shifting monitoring processes from an excessive concentration on source data verification to comprehensive risk-driven monitoring will increase efficiencies and enhance patient safety and data integrity while maintaining adherence to good clinical practice regulations. This philosophical shift in monitoring processes employs the addition of centralized and off-site mechanisms to monitor important trial parameters holistically, and it uses adaptive on-site monitoring to further support site processes, subject safety, and data quality. The main tenet is to use available data to monitor, assess, and mitigate the overall risk associated with clinical trials. Having the right technology is critical to collect and aggregate data, provide analytical capabilities, and track issues to demonstrate that a thorough quality management framework is in place. This paper lays out the high-level considerations when designing and building an integrated technology solution that will aid in scaling the methodology across an organization’s portfolio. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/therapeuticinnovationregulatoryscience-2014-barnes-536-45-technology-considerations-141022113727-conversion-gate01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> TransCelerate BioPharma Inc developed a methodology based on the notion that shifting monitoring processes from an excessive concentration on source data verification to comprehensive risk-driven monitoring will increase efficiencies and enhance patient safety and data integrity while maintaining adherence to good clinical practice regulations. This philosophical shift in monitoring processes employs the addition of centralized and off-site mechanisms to monitor important trial parameters holistically, and it uses adaptive on-site monitoring to further support site processes, subject safety, and data quality. The main tenet is to use available data to monitor, assess, and mitigate the overall risk associated with clinical trials. Having the right technology is critical to collect and aggregate data, provide analytical capabilities, and track issues to demonstrate that a thorough quality management framework is in place. This paper lays out the high-level considerations when designing and building an integrated technology solution that will aid in scaling the methodology across an organization’s portfolio.
Technology Considerations to Enable the Risk-Based Monitoring Methodology from www.datatrak.com
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How To Optimize Your EDC Solution For Risk Based Monitoring /slideshow/how-to-optimize-your-edc-solution-for-risk-based-monitoring-40600620/40600620 howtooptimizeyouredcsolutionforriskbasedmonitoring-141022111848-conversion-gate02
This presentation presents best training practices to leverage EDC technology and risk-based monitoring to effectively and efficiently monitor clinical research. Our focus is on the practical process of preparing your team to optimize the tools made available through an EDC solution. This presentation is applicable to CRA’s, clinical project managers, clinical data managers, regulatory compliance professionals, and those involved in the design and implementation of risked-based monitoring plans.]]>

This presentation presents best training practices to leverage EDC technology and risk-based monitoring to effectively and efficiently monitor clinical research. Our focus is on the practical process of preparing your team to optimize the tools made available through an EDC solution. This presentation is applicable to CRA’s, clinical project managers, clinical data managers, regulatory compliance professionals, and those involved in the design and implementation of risked-based monitoring plans.]]>
Wed, 22 Oct 2014 11:18:48 GMT /slideshow/how-to-optimize-your-edc-solution-for-risk-based-monitoring-40600620/40600620 DATATRAK@slideshare.net(DATATRAK) How To Optimize Your EDC Solution For Risk Based Monitoring DATATRAK This presentation presents best training practices to leverage EDC technology and risk-based monitoring to effectively and efficiently monitor clinical research. Our focus is on the practical process of preparing your team to optimize the tools made available through an EDC solution. This presentation is applicable to CRA’s, clinical project managers, clinical data managers, regulatory compliance professionals, and those involved in the design and implementation of risked-based monitoring plans. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/howtooptimizeyouredcsolutionforriskbasedmonitoring-141022111848-conversion-gate02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> This presentation presents best training practices to leverage EDC technology and risk-based monitoring to effectively and efficiently monitor clinical research. Our focus is on the practical process of preparing your team to optimize the tools made available through an EDC solution. This presentation is applicable to CRA’s, clinical project managers, clinical data managers, regulatory compliance professionals, and those involved in the design and implementation of risked-based monitoring plans.
How To Optimize Your EDC Solution For Risk Based Monitoring from www.datatrak.com
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eSource: What You Need To Know /slideshow/e-source-webinar/38149273 esourcewebinar-140819163946-phpapp01
View this recorded webinar to hear an overview of the Guidance Document on Electronic Source Data in Clinical Investigations and its practical implementation. ]]>

View this recorded webinar to hear an overview of the Guidance Document on Electronic Source Data in Clinical Investigations and its practical implementation. ]]>
Tue, 19 Aug 2014 16:39:46 GMT /slideshow/e-source-webinar/38149273 DATATRAK@slideshare.net(DATATRAK) eSource: What You Need To Know DATATRAK View this recorded webinar to hear an overview of the Guidance Document on Electronic Source Data in Clinical Investigations and its practical implementation. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/esourcewebinar-140819163946-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> View this recorded webinar to hear an overview of the Guidance Document on Electronic Source Data in Clinical Investigations and its practical implementation.
eSource: What You Need To Know from www.datatrak.com
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eSource: A Clinical Data Manager's Tale of Three Studies /slideshow/e-source-case-study-review/36568991 esourcecasestudyreview-140702161857-phpapp02
‘eSource: A Clinical Data Manager’s Tale of Three Studies’ highlights the challenges and benefits of eSource studies, and a look to the potential future. With the continuing adoption of eClinical solutions in clinical research, the need to understand, address, and utilize the time and cost savings benefits of eSource will grow increasingly important.]]>

‘eSource: A Clinical Data Manager’s Tale of Three Studies’ highlights the challenges and benefits of eSource studies, and a look to the potential future. With the continuing adoption of eClinical solutions in clinical research, the need to understand, address, and utilize the time and cost savings benefits of eSource will grow increasingly important.]]>
Wed, 02 Jul 2014 16:18:57 GMT /slideshow/e-source-case-study-review/36568991 DATATRAK@slideshare.net(DATATRAK) eSource: A Clinical Data Manager's Tale of Three Studies DATATRAK ‘eSource: A Clinical Data Manager’s Tale of Three Studies’ highlights the challenges and benefits of eSource studies, and a look to the potential future. With the continuing adoption of eClinical solutions in clinical research, the need to understand, address, and utilize the time and cost savings benefits of eSource will grow increasingly important. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/esourcecasestudyreview-140702161857-phpapp02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> ‘eSource: A Clinical Data Manager’s Tale of Three Studies’ highlights the challenges and benefits of eSource studies, and a look to the potential future. With the continuing adoption of eClinical solutions in clinical research, the need to understand, address, and utilize the time and cost savings benefits of eSource will grow increasingly important.
eSource: A Clinical Data Manager's Tale of Three Studies from www.datatrak.com
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Monitoring Plan Template /slideshow/monitoring-plan-template/35271844 monitoringplantemplate-140529124012-phpapp01
Use this template to create your Risk Based Monitoring guideline. Make sure you review this in conjunction with the Risk Based Monitoring in Practice presentation for the best possible result.]]>

Use this template to create your Risk Based Monitoring guideline. Make sure you review this in conjunction with the Risk Based Monitoring in Practice presentation for the best possible result.]]>
Thu, 29 May 2014 12:40:12 GMT /slideshow/monitoring-plan-template/35271844 DATATRAK@slideshare.net(DATATRAK) Monitoring Plan Template DATATRAK Use this template to create your Risk Based Monitoring guideline. Make sure you review this in conjunction with the Risk Based Monitoring in Practice presentation for the best possible result. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/monitoringplantemplate-140529124012-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Use this template to create your Risk Based Monitoring guideline. Make sure you review this in conjunction with the Risk Based Monitoring in Practice presentation for the best possible result.
Monitoring Plan Template from www.datatrak.com
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Risk Based Monitoring in Practice /slideshow/webinar-risk-based-approaches-to-clinical-monitoring/35271511 webinarrisk-basedapproachestoclinicalmonitoring-140529123226-phpapp01
After reviewing the FDA regulations on Risk Based Monitoring, review the details on how to put the principles into action! We include two reference documents to help you get started... and to make it a success.]]>

After reviewing the FDA regulations on Risk Based Monitoring, review the details on how to put the principles into action! We include two reference documents to help you get started... and to make it a success.]]>
Thu, 29 May 2014 12:32:26 GMT /slideshow/webinar-risk-based-approaches-to-clinical-monitoring/35271511 DATATRAK@slideshare.net(DATATRAK) Risk Based Monitoring in Practice DATATRAK After reviewing the FDA regulations on Risk Based Monitoring, review the details on how to put the principles into action! We include two reference documents to help you get started... and to make it a success. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/webinarrisk-basedapproachestoclinicalmonitoring-140529123226-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> After reviewing the FDA regulations on Risk Based Monitoring, review the details on how to put the principles into action! We include two reference documents to help you get started... and to make it a success.
Risk Based Monitoring in Practice from www.datatrak.com
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Gamification to Incentivize Sites ACRP 2014 /slideshow/gamification-to-incentivize-sites-acrp/34420310 gamificationtoincentivizesitesacrp-140507225247-phpapp02
Niki Kutac, Director Product Management, delivered this presentation at the ACRP 2014 Conference where it was rated the #1 Session of the Event. Learn how to implement gamification to produce the desired end result.]]>

Niki Kutac, Director Product Management, delivered this presentation at the ACRP 2014 Conference where it was rated the #1 Session of the Event. Learn how to implement gamification to produce the desired end result.]]>
Wed, 07 May 2014 22:52:47 GMT /slideshow/gamification-to-incentivize-sites-acrp/34420310 DATATRAK@slideshare.net(DATATRAK) Gamification to Incentivize Sites ACRP 2014 DATATRAK Niki Kutac, Director Product Management, delivered this presentation at the ACRP 2014 Conference where it was rated the #1 Session of the Event. Learn how to implement gamification to produce the desired end result. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/gamificationtoincentivizesitesacrp-140507225247-phpapp02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Niki Kutac, Director Product Management, delivered this presentation at the ACRP 2014 Conference where it was rated the #1 Session of the Event. Learn how to implement gamification to produce the desired end result.
Gamification to Incentivize Sites ACRP 2014 from www.datatrak.com
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Using Gamification to Incentivize Sites /slideshow/gamification-to-incentivize-sites/32784580 diaeuromeetinggamification-140326181711-phpapp01
Gamification is a popular tool to improve site performance. Find out how to use it get the maximum benefit.]]>

Gamification is a popular tool to improve site performance. Find out how to use it get the maximum benefit.]]>
Wed, 26 Mar 2014 18:17:11 GMT /slideshow/gamification-to-incentivize-sites/32784580 DATATRAK@slideshare.net(DATATRAK) Using Gamification to Incentivize Sites DATATRAK Gamification is a popular tool to improve site performance. Find out how to use it get the maximum benefit. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/diaeuromeetinggamification-140326181711-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Gamification is a popular tool to improve site performance. Find out how to use it get the maximum benefit.
Using Gamification to Incentivize Sites from www.datatrak.com
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Utilizing a Unified Platform to Bridge Geographical and Departmental Gaps While Expediting an Entire Development Program /slideshow/dia-japan-jan-2014-presentation-bill-gluck/30951505 diajapan-jan2014presentation-billgluck-140207102603-phpapp02
Presentation discusses: The Drug Development Process The Drug Development Paradox Regulations and Guidelines Standards - CDISC Leveraging Technology Resource Management ]]>

Presentation discusses: The Drug Development Process The Drug Development Paradox Regulations and Guidelines Standards - CDISC Leveraging Technology Resource Management ]]>
Fri, 07 Feb 2014 10:26:03 GMT /slideshow/dia-japan-jan-2014-presentation-bill-gluck/30951505 DATATRAK@slideshare.net(DATATRAK) Utilizing a Unified Platform to Bridge Geographical and Departmental Gaps While Expediting an Entire Development Program DATATRAK Presentation discusses: The Drug Development Process The Drug Development Paradox Regulations and Guidelines Standards - CDISC Leveraging Technology Resource Management <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/diajapan-jan2014presentation-billgluck-140207102603-phpapp02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Presentation discusses: The Drug Development Process The Drug Development Paradox Regulations and Guidelines Standards - CDISC Leveraging Technology Resource Management
Utilizing a Unified Platform to Bridge Geographical and Departmental Gaps While Expediting an Entire Development Program from www.datatrak.com
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Mitigating Risks in Clinical Studies /slideshow/mitigating-risks-in-clinical-studies/18628181 mitigatingriskinclinicalstudies-130411125422-phpapp01
In the course of any clinical trial, there are risks associated with specific activities and tasks. This webinar will highlight some of these key risk areas and provide guidance on combining technology with best practices to help mitigate risks. ]]>

In the course of any clinical trial, there are risks associated with specific activities and tasks. This webinar will highlight some of these key risk areas and provide guidance on combining technology with best practices to help mitigate risks. ]]>
Thu, 11 Apr 2013 12:54:22 GMT /slideshow/mitigating-risks-in-clinical-studies/18628181 DATATRAK@slideshare.net(DATATRAK) Mitigating Risks in Clinical Studies DATATRAK In the course of any clinical trial, there are risks associated with specific activities and tasks. This webinar will highlight some of these key risk areas and provide guidance on combining technology with best practices to help mitigate risks. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/mitigatingriskinclinicalstudies-130411125422-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> In the course of any clinical trial, there are risks associated with specific activities and tasks. This webinar will highlight some of these key risk areas and provide guidance on combining technology with best practices to help mitigate risks.
Mitigating Risks in Clinical Studies from www.datatrak.com
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Using Technology to Integrate Clinical Data Management and Clinical Operations /slideshow/using-technology-to-integrate-clinical-data-management-and-clinical-operations/17719961 acdm-3-2-2013-gluck-130326112213-phpapp01
Historical Perspectives Integrating Clinical Operations Integrating Clinical Data Management Case Study Examples Conclusions and Parting Thoughts ]]>

Historical Perspectives Integrating Clinical Operations Integrating Clinical Data Management Case Study Examples Conclusions and Parting Thoughts ]]>
Tue, 26 Mar 2013 11:22:13 GMT /slideshow/using-technology-to-integrate-clinical-data-management-and-clinical-operations/17719961 DATATRAK@slideshare.net(DATATRAK) Using Technology to Integrate Clinical Data Management and Clinical Operations DATATRAK Historical Perspectives Integrating Clinical Operations Integrating Clinical Data Management Case Study Examples Conclusions and Parting Thoughts <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/acdm-3-2-2013-gluck-130326112213-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Historical Perspectives Integrating Clinical Operations Integrating Clinical Data Management Case Study Examples Conclusions and Parting Thoughts
Using Technology to Integrate Clinical Data Management and Clinical Operations from www.datatrak.com
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Streamlining Mid-Study Changes with Technology /DATATRAK/streamlining-midstudy-changes-with-technology midstudychangeshimss-v5-130228101744-phpapp02
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Thu, 28 Feb 2013 10:17:44 GMT /DATATRAK/streamlining-midstudy-changes-with-technology DATATRAK@slideshare.net(DATATRAK) Streamlining Mid-Study Changes with Technology DATATRAK <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/midstudychangeshimss-v5-130228101744-phpapp02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br>
Streamlining Mid-Study Changes with Technology from www.datatrak.com
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The FDA Guidance of a Risk-Based Approach to Monitoring as Viewed By CDM /slideshow/the-fda-guidance-of-a-riskbased-approach-to-monitoring-as-viewed-by-cdm/16507187 dia-japan-gluck-session5-130213092120-phpapp02
Historical Perspectives in CDM Overview of the Draft Guidance A Risked-Based Approach Challenges to a Risk-Based Approach Supporting a Risked-Based Approach ]]>

Historical Perspectives in CDM Overview of the Draft Guidance A Risked-Based Approach Challenges to a Risk-Based Approach Supporting a Risked-Based Approach ]]>
Wed, 13 Feb 2013 09:21:20 GMT /slideshow/the-fda-guidance-of-a-riskbased-approach-to-monitoring-as-viewed-by-cdm/16507187 DATATRAK@slideshare.net(DATATRAK) The FDA Guidance of a Risk-Based Approach to Monitoring as Viewed By CDM DATATRAK Historical Perspectives in CDM Overview of the Draft Guidance A Risked-Based Approach Challenges to a Risk-Based Approach Supporting a Risked-Based Approach <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/dia-japan-gluck-session5-130213092120-phpapp02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Historical Perspectives in CDM Overview of the Draft Guidance A Risked-Based Approach Challenges to a Risk-Based Approach Supporting a Risked-Based Approach
The FDA Guidance of a Risk-Based Approach to Monitoring as Viewed By CDM from www.datatrak.com
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CDM's Role in Supporting Risk-Based Monitoring /slideshow/cdms-role-in-supporting-riskbased-monitoring/15035513 10gluckcdmrolesupportingrisk-basedmonitoring-11-3-2012-121105130048-phpapp01
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Mon, 05 Nov 2012 13:00:46 GMT /slideshow/cdms-role-in-supporting-riskbased-monitoring/15035513 DATATRAK@slideshare.net(DATATRAK) CDM's Role in Supporting Risk-Based Monitoring DATATRAK <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/10gluckcdmrolesupportingrisk-basedmonitoring-11-3-2012-121105130048-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br>
CDM's Role in Supporting Risk-Based Monitoring from www.datatrak.com
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Understanding the Cloud /slideshow/understanding-thecloud/14687921 understandingthecloud-121011120649-phpapp02
Learn the basics of cloud computing today. Understand the benefits the cloud can provide your business and what it means for your data.]]>

Learn the basics of cloud computing today. Understand the benefits the cloud can provide your business and what it means for your data.]]>
Thu, 11 Oct 2012 12:06:46 GMT /slideshow/understanding-thecloud/14687921 DATATRAK@slideshare.net(DATATRAK) Understanding the Cloud DATATRAK Learn the basics of cloud computing today. Understand the benefits the cloud can provide your business and what it means for your data. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/understandingthecloud-121011120649-phpapp02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> Learn the basics of cloud computing today. Understand the benefits the cloud can provide your business and what it means for your data.
Understanding the Cloud from www.datatrak.com
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Innovative Learning Opportunities: A Collaboration between Industry and Academia /slideshow/innovative-learning-opportunities-a-collaboration-between-industry-and-academia/13618180 gluckwdia2012-120712104030-phpapp01
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Thu, 12 Jul 2012 10:40:28 GMT /slideshow/innovative-learning-opportunities-a-collaboration-between-industry-and-academia/13618180 DATATRAK@slideshare.net(DATATRAK) Innovative Learning Opportunities: A Collaboration between Industry and Academia DATATRAK <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/gluckwdia2012-120712104030-phpapp01-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br>
Innovative Learning Opportunities: A Collaboration between Industry and Academia from www.datatrak.com
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Integrating Clinical Operations and Clinical Data Management Through EDC /slideshow/integrating-clinical-operations-and-clinical-data-management-through-edc/12211036 marchwebinar-3-29-2012-120329112943-phpapp02
When electronic data capture was first introduced there was a great deal of discussion surrounding how the technology would alter the roles of those in clinical operations and clinical data management. Through the review of a case study, we will explore how EDC is used as a tool to more tightly integrate clinical operational staffs with those in clinical data management resulting in a more streamlined process from study initiation to database lock.]]>

When electronic data capture was first introduced there was a great deal of discussion surrounding how the technology would alter the roles of those in clinical operations and clinical data management. Through the review of a case study, we will explore how EDC is used as a tool to more tightly integrate clinical operational staffs with those in clinical data management resulting in a more streamlined process from study initiation to database lock.]]>
Thu, 29 Mar 2012 11:29:41 GMT /slideshow/integrating-clinical-operations-and-clinical-data-management-through-edc/12211036 DATATRAK@slideshare.net(DATATRAK) Integrating Clinical Operations and Clinical Data Management Through EDC DATATRAK When electronic data capture was first introduced there was a great deal of discussion surrounding how the technology would alter the roles of those in clinical operations and clinical data management. Through the review of a case study, we will explore how EDC is used as a tool to more tightly integrate clinical operational staffs with those in clinical data management resulting in a more streamlined process from study initiation to database lock. <img style="border:1px solid #C3E6D8;float:right;" alt="" src="https://cdn.slidesharecdn.com/ss_thumbnails/marchwebinar-3-29-2012-120329112943-phpapp02-thumbnail.jpg?width=120&amp;height=120&amp;fit=bounds" /><br> When electronic data capture was first introduced there was a great deal of discussion surrounding how the technology would alter the roles of those in clinical operations and clinical data management. Through the review of a case study, we will explore how EDC is used as a tool to more tightly integrate clinical operational staffs with those in clinical data management resulting in a more streamlined process from study initiation to database lock.
Integrating Clinical Operations and Clinical Data Management Through EDC from www.datatrak.com
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https://cdn.slidesharecdn.com/profile-photo-DATATRAK-48x48.jpg?cb=1522868980 www.datatrak.com https://cdn.slidesharecdn.com/ss_thumbnails/cbiesourcepresentationbillgluckfinal-150508153523-lva1-app6892-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/cbi-e-source-presentation-bill-gluck-final/47916431 eSource: Data Capture ... https://cdn.slidesharecdn.com/ss_thumbnails/mitigateriskwebinar-3-25-2015-150325150016-conversion-gate01-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/leverage-your-edc-solution-to-mitigate-risk-in-clinical-research-46286041/46286041 Leverage Your EDC Solu... https://cdn.slidesharecdn.com/ss_thumbnails/therapeuticinnovationregulatoryscience-2014-wilson-529-35-defining-central-monitoring-capability-141022114912-conversion-gate01-thumbnail.jpg?width=320&height=320&fit=bounds slideshow/therapeutic-innovation-regulatory-science-2014wilson52935definingcentralmonitoringcapability/40601926 Defining a Central Mon...