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Results for: Consulting - Regulatory

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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  • Sustainable Compliance Begins with a Strong Foundation

    Brochure — December 8, 2011
    The urgency of a problem often entices people to quickly focus on finding a solution and repairing the problem in order to immediately remedy the situation.

  • Quintiles Names Rick Sax New Head of Integrated Clinical Services

    Press Release — May 23, 2011 – Quintiles announced the appointment of Frederic “Rick” Sax as Senior Vice President and Global Head of its Integrated Clinical Services division.rograms.

  • Advancing Vaccine Development in Australia and New Zealand

    Case Study — April 11, 2011
    Quintiles rose to the challenge of a very aggressive vaccine recruitment timeline during the holiday period - and recruited 3,000+ subjects from 18-90 years of age within just 17 days - 25 days ahead of schedule.

  • Clinical Endpoint Committees

    White Paper — February 22, 2011
    As regulatory boards are expecting more from clinical endpoint committees, what guidance can you follow? This white paper sets forth current best practice for CECs.

  • 25 Years of Regulation - and Still Failing - Risky Business, Chapter 4

    Hear from the Experts — February 2, 2011
    Chapter Excerpt from Risky Business: Managing the Quality of America’s Medicines Chapter four identifies two simple principles needed for the improvement of quality management in pharmaceuticals today: managing consistency and maintaining responsiveness.

  • Responding to FDA Enforcement

    Brochure — October 5, 2010
    As the FDA ratchets up its enforcement actions, pharmaceutical and medical device companies are turning to Quintiles. Learn what differentiates our consulting solutions.

  • Reinventing Safety

    Brochure — September 22, 2010
    When you integrate all your safety information, you can make better decisions, navigate regulatory hurdles and get to market faster.

  • Scaling Up for Safety: How to Gain Efficiencies without Sacrificing Quality

    Case Study — September 16, 2010
    Read how Quintiles set-up a complete pharmacovigilance operation in a developing region in only six months for a leading pharma company.

  • Safety Strategy & Optimization

    Brochure — September 14, 2010
    Learn how to enable your safety group to become a value-added contributor throughout the product lifecycle.

  • Managing Pharmacovigilance as a Business

    White Paper — July 28, 2010
    The three steps required to develop a strategic approach to global capacity management.

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