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Results for: Case Studies - Europe - North and Central America

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  • Energizing Enrollment

    October 4, 2011
    The rapid recruitment for this Phase III, open, randomized, controlled, multi-center study in adjuvant triple-negative breast cancer (TNBC) was completed two months earlier than planned.

  • Constant Vigilance

    March 16, 2011
    Centralized planning played a key role in improving productivity during site visits and close monitoring ensured the high standards Quintiles put in place were met.

  • Scientific Bulletin Flow Cytometry

    February 9, 2011
    Quintiles has expertise in running highly regulated flow cytometry assays, as well as a number of esoteric assays, such as multicolor cell surface and intracellular staining assays, and receptor occupancy/competitive binding assays.

  • Competitive Edge - Ulcerative Colitis

    February 2, 2011
    Although faced with the challenge of recruiting for this small patient population, enrollment was completed two months ahead of schedule.

  • Superior Teamwork - Renal Transplants

    February 2, 2011
    901 patients were randomized according to the protocol timelines. The database lock was achieved 11 days before the original target date.

  • Epilepsy - Refining Recruitment

    February 1, 2011
    Quintiles provided clinical monitoring and project management for a randomized, double-blind, parallel-group, placebo and comparator controlled multicenter study of Drug X in patients with epilepsy.

  • Global Response HIV

    February 1, 2011
    Due to its global reach and extensive experience, Quintiles successfully managed 830 sites in 32 countries and recruited 14,521 patients.

  • Acute Coronary Syndrome - Tailored Solutions

    February 1, 2011
    Find out how our experience in multi-national cardiovascular clinical trials helped this customer reach database lock 66 days after LPO.

  • Managing Trauma

    September 14, 2010
    Quintiles overcame the unpredictability of patient recruitment due to the emergency setup and the client was able to file for approval based on phase II data only.

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