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Brochures - Data Management

To learn more about a particular aspect of Quintiles’ pharma services, biotech development or drug commercialization services, select a topic at left. If you’ve already specified a choice, you may narrow your search by selecting additional categories in any order. For example, for information on oncology drug development, start by selecting oncology. Then you can narrow your search to Central Lab, News Releases and Europe.

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  • 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.

  • Centralized Data Access for Total Study Control

    November 18, 2009
    Quintiles’ Interactive Response Technology (IRT) platform SEAMLESSLY integrates patient interaction systems for clinical development with the supply chain services of clinical labeling, packaging and distribution.

  • CDSIC – Electronic data submission

    August 13, 2009
    There is an increasing global requirement for Clinical Data Interchange Standards Consortium (CDISC) -based standardized data for regulatory submissions.

  • Clinical Development Services

    June 18, 2009
    Find out how large pharmaceutical companies and emerging biotech move products past each development milestone.

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