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临床Trial Project Management and Monitoring
一个接触点。和你在一起的方式。
前期规划导致更少的延迟和学习errors, assuring you receive high-quality study outcomes. Our clinical trial management philosophy supports all aspects of your early clinical trials cost effectively with clear roles and responsibilities.
是否使用我们临床研究中心or our qualified external sites, your project manager is a key resource in managing your study. These seasoned professionals, with relevant scientific and therapeutic expertise, serve as your central contact throughout the entire process.
Let us help you:
- 制定项目计划和时间表
- 启动活动和研究启动
- 监督学习行为和临床监测
- 管理协议开发的数据支持团队到临床研究报告
- 维持和报告药物测量物品可交付成果
- 选择和管理供应商
一个细节。精确递送。
它需要特殊的人来监测临床试验。在一瞬间通知时，个人有灵活性地跳上飞机，并有了一个细节，并对法规和良好的临床实践进行广泛了解。我们独立的临床试验监测器确保您的研究符合多种规定。我们保护受试者的权利，并确保从源数据准确，完整和可核实的学习数据。
You have access to a network of CRAs experienced in monitoring early phase trials from first-in-human through PoC, in settings including Covance CRUs, external CRUs, hospitals, specialized research centers and medical practice settings.