精确设计您的临床试验

准确地预测研究时间表和预算的同时优化性能,利用使您能够降低设计复杂性,缩短临床开发周期并提高试验成功的可能性的工具。

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Orchestrate better study outcomes right from the start.

通过IQVIA Planning Suite成功地解决了您最关键的研究设计决策点 - 由IQVIA Connected Intelligence™驱动。

优化从协议设计,可行性和现场选择到患者入学和课程校正的开发活动。以无与伦比的准确性预测操作执行和预算。保持学习的正轨。

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更可预测

study performance Up to 40% reduction in protocol amendments
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Faster cycle times

站点选择完成加速30天
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Heightened accuracy

Grantplan是世界上最大,最准确的试验预算工具,用于76%的全球临床试验。
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Greater efficiency

减少了非注册站点的数量(> 40%的总数),避免了每个发起站点$ 30K的成本。
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改进的网站/患者经验

更快的现场调查完成13天;患者负担得分最高可降低24%
活动时间表设计师

Design an optimal schedule of trial activities to accurately predict and heighten study performance.

  • 更好地评估协议设计并降低昂贵修订的风险。
  • Create and compare multiple scenarios and model cost tradeoffs, reducing risk and expenditures, improving the site and patient experience and decreasing study timelines.
  • 通过识别和删除不必要的审判程序和访问来简化活动时间表。
  • Reduce site and patient burden by highlighting and eliminating barriers to participation and satisfaction.

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数据查询系统

利用我们干净,多源,易于搜索的全球数据存储库,将研究计划优化,并更好地匹配研究人员和站点与试验目标。

  • World’s largest and most up-to-date historical performance and Site repository.
  • Results in smarter list of sites built on an integrated view that reduces time/costs of selecting sites, avoids/minimizes non-performing sites and increases investigator engagement.
  • Inter-company and sponsor/CRO data sharing arrangements possible for heightened performance.

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Study Optimizer

More predictably plan, manage, and flexibly re-forecast patient enrollment scenarios

  • Designed to handle study complexities and multiple operating models.
  • 缩短时间表并优化操作执行。
  • 压力测试CRO出价以验证入学人数可行性。
  • Keeps you on top of study enrollment progress via real-time data feeds.
  • Provides early insights into potential risks or delays; enables rescue strategy modeling.

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Feasibilty

Employ strategic, data-driven feasibility regarding trial strategy and planning, protocol finalization, and selection of the most appropriate countries and sites.

  • 由于使用拟合技术和自动化,驱动器被证明,加速的结果。
  • Improves country and target site identification and information gathering.
    • 精简CDA谈判
    • 驱动更快的调查完成和现场选择过程
  • Heightens investigator experience and loyalty.

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赠款计划

在所有试验阶段,指示和国家 /地区,有效,准确和确定的预算

  • Employ the industry’s largest, most efficient and accurate clinical budgeting tool Leverage line-item costs at fair market value to accurately build and adjust study budgets and boost compliance.
  • Leverage line-item costs at fair market value to accurately build and adjust study budgets and boost compliance.
  • Streamline, simplify and accelerate investigator negotiations.
  • 最新信息将不断扩展和刷新季度。
  • Standard of Care module helps avoid supplicate spending on insurance-covered procedures. View previously agreed site-level budget iterations.
  • 也可用:研究人员发起的研究(GPI)的赠款计划,这是专为研究人员发起的研究而构建的唯一工具。

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Better addressing trial delays and cost overruns means designing and planning your studies early, often and comprehensively.

研发技术解决方案副总裁Melissa Easy

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