Medidata Solutions, Tessella and United BioSource Corporation to Deliver Third Webinar in Series on Adaptive Clinical Trials



    September 12th Installment to Focus on EDC & CDMS in Adaptive Clinical
    Trials

    NEW YORK, Aug. 30 /CNW/ - Medidata Solutions, Tessella and United
BioSource Corporation:

    
    WHO:     Hugh Levaux, Ph.D., Vice President of Product Strategy,
             Medidata Solutions
             Tom Parke, Head of Clinical Trial Solutions, Tessella
             Mike Borkowski, General Manager of Clinical Technologies
             Group, UBC

    WHAT:    "Enabling Adaptive Clinical Trials: Electronic Data Capture
             & Clinical Data Management Systems"
             In the third installment of the "Enabling Adaptive Clinical
             Trials" six-part series, Medidata Solutions, Tessella and
             UBC will lead a discussion exploring the critical role of EDC
             and CDM systems in executing adaptive clinical trials.
             Presenters will discuss requirements for these systems, and
             will examine the implications around data handling, security,
             and metadata integrations to ensure optimal trials.

    WHEN:    Wednesday, September 12th, 9-10 a.m. ET, 2-3 p.m. ET
             and 7-8 p.m. ET

    WHERE:   Participants are asked to register by 12 p.m. ET on
             September 7th at: www.enablingadaptivetrials.com
    

    About Tessella

    Since 1998, Tessella has been helping to drive innovation in drug
development by enabling the deployment of Bayesian-based adaptive clinical
trials. Tessella has implemented statistical models for phase 1 trials, phase
2 dose finding studies using Bayesian statistics, and phase 2/3 seamless
designs. Tessella has supported these models by developing simulation and
analysis tools, and by building and running the infrastructure to run the
trials. For more information, please visit www.tessella.com/adaptivedesigns.

    About UBC

    UBC is a global pharmaceutical services organization that combines deep
scientific knowledge with broad execution expertise across the lifecycle
continuum. Our focus is on generating real-world data to support the
development and commercialization of medical products for emerging and
established life science companies. We partner with our clients to offer
services in scientific research and consulting, late stage development,
post-approval registries and drug safety, data integration, clinical
technologies, investigator services, patient recruiting and education. For
more information, please visit www.unitedbiosource.com.

    About Medidata Solutions Worldwide

    Medidata Solutions helps the world's leading pharmaceutical,
biotechnology, medical device and research organizations maximize the value of
their clinical research investments. Innovative process design, technology and
services streamline clinical trials by providing early visibility to reliable
clinical data - the lifeblood of every research organization. Working with
companies and institutions both large and small, Medidata Solutions helps
clinical researchers safely accelerate the process of bringing life-enhancing
treatments to market - on six continents and in more than 80 countries.
Medidata Solutions brings significant value to its broad client base with deep
clinical experience and expertise in more than 20 therapeutic areas, projects
in Phase I, II, III, IV, registries and surveillance, and studies with
thousands of investigators and tens-of-thousands of subjects. For more
information, please visit www.mdsol.com.




For further information:

For further information: Medidata Contact: Lois Paul & Partners Susan
Lombardo, 781-782-5767 Susan_Lombardo@lpp.com or Tessella Contact: Tessella
Emily Turberville-Tully, +44(0)1235-555511
Emily.Turberville-Tully@tessella.com or UBC Contact: United BioSource
Corporation Tess Drahzal, 240-644-0420 Tess.Drahzal@unitedbiosource.com

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MEDIDATA SOLUTIONS WORLDWIDE

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