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  • Real-World & Late Phase Research

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  • Quintiles Clinical Trial

    The demand for real-world research about your product never stops.  How can you best develop your evidence portfolio?

    Either peri- or post-approval, your product raises new questions for regulatory, payers, providers and patients. Observational outcomes in real-world settings can satisfy their need to know more about safety, effectiveness, and quality.  Quintiles offers unmatched expertise in the full range of observational and real-world research:

    • Patient registries - Experience in conducting more than 220 registries including product, disease and pregnancy registries in over 80 countries
    • Quality of life and patient-reported outcomes – Evidence to support benefits/claims in product labeling
    • Safety outcomes / REMS – Safety and risk monitoring over longer periods; also monitoring off-label use
    • Comparative effectiveness – Studies to provide evidence of effectiveness in different populations
    • Health outcomes / health economics – Critical support for formulary approval or reimbursement efforts
    • Retrospective data collection – Our databases and networks give access to 60 million patient records
    Quintiles Infosario Outcomes seal

  • Expertise in demonstrating real-world effectiveness and safety

  • Quintiles Clinical Trails

    As healthcare stakeholders increasingly seek evidence to support regulatory, reimbursement and prescribing decisions, real-world and late phase research is becoming critical to ensuring the success of a product. Read brochure

  • Quintiles Clinical Trails

    Learn more about evaluating safety in the post-marketing setting, and variety of approaches for obtaining safety data in the post-marketing setting, including most commonly, observational studies that inform stakeholders, including manufacturers, healthcare providers, and patients, about the benefit-risk profile for medicinal products in the real world. View Webinar