Quintiles.com

  • Safety and Pharmacovigilance

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  • Quintiles Clinical Trial

    The stakes are higher than ever for safety and risk management. Improving outcomes requires more agile coordination than traditional safety systems can provide.

    That’s why Quintiles created Lifecycle Safety, a multi-dimensional approach to integrating safety activities across functions and phases. From early development through post-marketing, we can help you manage risk and make better decisions about your product’s future.

    Transform pharmacovigilance compliance into competitive advantage with Lifecycle Safety

    We combine 30 years’ experience and proven processes with best-in-class safety management technology to help you:
    • Efficiently monitor safety and manage case reports and adverse event reporting on a global scale 
    • Identify and characterize risk earlier in your development
    • Manage and maximize your product's risk-benefit profile 
    • Improve the market value of your product with proactive planning and robust risk-benefit management 

  • Lifecycle safety insights for better risk management

  • Quintiles Clinical Trails

    Our global team of operational, strategic, scientific, legal, regulatory and quality experts are focused on safety/benefit-risk have been trained to meet global regulatory requirements with quality cost-effective approaches. 

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  • Quintiles Clinical Trails

    When you integrate all your safety information, you can make better decisions, navigate regulatory hurdles and get to market faster.
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  • Quintiles Clinical Trails

    Quintiles' comprehensive aggregate reporting and analytics solutions, which are fully scalable and customizable, will empower you to meet increasing regulatory demands and make informed decisions about your product sooner.  Learn More

  • Quintiles Clinical Trails

    In the increasingly scrutinized and budget-constrained environment of the New Health, the pharmacovigilance function must be as compliant and cost-effective as possible.
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