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White Papers - Thought leadership

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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  • Title
  • Shaping Clinical Transformation

    November 18, 2009
    A summary of key insights exchanged between pharma executives at the inaugural Quintiles Consulting Executive Vision Forum.

  • Rewarding Innovation and Value: What is the Role of Comparative Effectiveness Research

    October 6, 2009
    The impact of comparative effectiveness research on the future of drug development.

  • Rebalancing Risk to Transform R&D

    June 3, 2009
    A strategic approach to re-balancing the main components of biopharma company risk: portfolio, operational and resource.

  • The Value of CROs

    March 31, 2009
    Contract Research Organizations (CROs) are making an increasingly valuable contribution to healthcare by conducting the clinical trials that help determine which investigational medicines advance toward regulatory approval.

  • The New Face of Clinical Data Management

    March 31, 2009
    Discusses the new face of clinical data management in today's biopharmaceutical industry.

  • Reinventing the Clinical Trial

    March 31, 2009
    As a new era of drug discovery unfolds, reinventing the clinical trial is essential to medical advancement.

  • The Globalization of Clinical Trials

    March 31, 2009
    Today, the globalization of clinical trials is accelerating, driven by scientific and economic needs to reach more patients.

  • Championing the Clinical Trial

    March 31, 2009
    Quintiles’ ethical standards and review procedures ensure patient safety remains the top priority for all clinical trials. The company is also leading the way for data transparency, so drug trial sponsors have instant access to information about the conduct and status of trials.

  • Advancing Drug Development Through Pharmacogenomics

    March 31, 2009
    Pharmacogenomics (PG x) is the study of how such genetic differences influence drug therapy. The goal is to use a person’s DNA profile to predict how the individual will respond to a medicine. The ability to predict drug response holds enormous promise to advance the drug development process and to improve drug safety and effectiveness in medical practice.