1. Powering Pediatrics Studies: Meeting the FDA's Pharmacometrics Criteria Using Phoenix NLME & Trial Simulator


    from Certara / Added

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    Effective medications are a mainstay of modern pediatric medicine. Yet, ethical concerns about conducting clinical trials in pediatric patients are a major challenge in pediatric drug development. Learn how Dr. Samer Mouksassi and his team at Pharsight Consulting Services have overcome these challenges through the use of pharmacometrics.

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    • A first look at Phoenix Trial Designer, the successor to Trial Simulator


      from Certara / Added

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      This webinar will demonstrate a simulation of a case study using the prototype of Phoenix Trial Designer, which is actively being developed by Certara. The webinar will update interested users on the progress of the software, show the proposed design of the tool, discuss its dependencies, and outline intended capabilities for the first version of this product. Future plans for the tool following the first release will also be discussed. To help guide decisions on the development of this product, we will gather feedback from M&S scientists attending this webinar in a Q&A session. The intended audience is scientists familiar with Pharsight Trial Simulator who are interested in the successor software, Phoenix Trial Designer.

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      • Orphan Drug Congress Nov 2013: Part 3, How to Help Inexperienced Sites Conduct Successful Studies


        from Premier Research / Added

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        WODC Europe Panel Discussion Making Clinical Trials Feasible November 14, 2013 Part 3: How to Help Inexperienced Sites Conduct Successful Studies

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        • Orphan Drug Congress April 2013: Part 1, Approaches to Clinical Trial Design


          from Premier Research / Added

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          Approaches to Clinical Trial Design: Biomarkers, Adaptive Design, etc. Learn more about our Rare Disease and Orphan Drug Development capabilities here: http://premier-research.com/our-experience/rare-disease/

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          • CTTI Central IRB Recommendations Could Speed Development of New Medical Therapies


            from CTTI / Added

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            CTTI central IRB recommendations could speed development of new medical therapies by eliminating inefficiencies. This video pertains to CTTI's Central IRB Project: http://www.ctti-clinicaltrials.org/what-we-do/study-start/central-irb *The views and opinions expressed in this video are those of the speaker and do not necessarily reflect the official policy or position of CTTI.

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