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Results for: Brochures - Cost control/reduction - Clinical Services

In the complex environment of the New Health, Quintiles is committed to helping you succeed. At every stage of your product’s lifecycle, we are dedicated to delivering real results, being proactive in navigating issues and thinking of new solutions.  Search our library today.

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  • Quintiles Infosario Streamlining Trials with Better Communication

    March 12, 2012
    The Quintiles Infosario™ Investigator Portal fundamentally changes the way clinical trial lab work is managed. Putting timely laboratory data at the fingertips of investigators, this advanced system offers greater transparency and efficiency to tighten study timelines and increase the quality of data.

  • Quintiles Infosario Clinical Trial Management System Fact Sheet

    January 17, 2012
    A fully hosted, global Clinical Trial Management System(CTMS) that provides scalable functionality across multiple business processes. A key component of our Systems as a Service offering, the Quintiles Infosario CTMS provides a centralized location for capturing, viewing, and sharing clinical trial data—from site identification to study closeout.

  • Quintiles Infosario

    June 10, 2011
    Quintiles Infosario™ is a new, comprehensive suite of services that enables optimized drug development.

  • Systems as a Service

    June 3, 2011
    Quintiles Infosario™ Systems as a Service gives you access to our best-of-breed commercial platforms and proprietary technologies, augmented by Quintiles’ leading clinical expertise.

  • Population PK/PD - Modeling and Simulation Optimization Tools

    February 11, 2011
    Population pharmacokinetic/ pharmacodynamic (PK/PD) modeling and simulation, available from Quintiles, is now endorsed by the FDA as often being instrumental in drug approval and labeling.

  • BIOS Standardize Data with SPARC

    February 2, 2010
    There is an increasing global requirement for Clinical Data Interchange Standards Consortium (CDISC) -based standardized data for regulatory submissions. At Quintiles, we have proactively addressed this need by training our staff, gaining experience, and developing and implementing innovative solutions for creating data that adhere to current CDISC Study Data Tabulation Model (SDTM) specifications.

  • Sub-Saharan Africa Phase II/III Fact Sheet

    July 29, 2009
    Sub-Saharan Africa fact sheet about Phase II/III trials. The gateway to Africa: Access to expanded clinical resources and patient populations in South Africa and beyond.

  • Risk Assessment & Strategy

    April 16, 2009
    Quintiles benefit risk analysis can help you anticipate potential regulatory concerns and highlight the benefit side of your drug’s benefit risk profile.

  • How to Navigate the New CDISC Standard

    March 25, 2009
    Quintiles – a CDISC Registered Solutions Provider – helps you get every detail right.

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