临床数据管理分析和报告

We partner with you to provide accurate, insightful clinical trial data management from the moment it’s recorded to the moment it’s reported.

  • 临床trial databases go into production on time, 94% of the time

  • Seamless integration of clinical data through synchronized platforms

  • Proactive targeting of potential problem areas

临床data management and analysis at Covance. Photo of a scientist sitting at a workstation.
Your Needs

We provide准确的阴茎数据从录制到它的报告时间的那一刻起。通过使用共同的全局平台和统一流程,我们能够向您保证,您可以获得最高的全球数据质量。

我们的全球基础架构,工作流程和informatics platform为您提供24小时时钟的福利。而且,由于我们的团队都受过培训和舒适的过程,因此您将受益于全球团队的互换性。

There are a lot of moving parts with complex, global clinical trials. We have a specially dedicated team responsible for coordinating both internal and external communication. This enables easy access to subject matter experts and higher quality output, every time.

我们的能力

Having the internal sources to manage all the data a clinical trial generates can be difficult. Covance can assist you withclinical data managementevery step of the way — from the point it’s first collected to warehousing it. And to ensure seamless integration of your data, our teams are all trained in same processes.

You may engage us for stand-alone, full-service or functional outsourcing in the following disciplines:

  • 协议设计与评论
  • Randomization schedules
  • 案例报告表格(CRF)设计和审查
  • 数据库设计
  • 数据输入
  • 数据验证/验证
  • Data transfer
  • Medical coding
  • Quality management procedures
  • Data manipulation
  • EDC

我们帮助您定义正确的研究组件以获得最佳效率,然后通过以确保临床结果符合您的目标。

高级编程解决方案可提高效率,在一项研究中或在许多研究中:

  • Statistical analysis plans
  • 安全性和疗效的综合摘要
  • 表格,数字和列表
  • 随机化代码代
  • 统计和临床研究报告
  • Publication and abstract support
  • 药物经济,QOL分析
  • 中学评估包括临时分析
  • Data safety monitoring boards (DSMBs)
  • Set-up, charter, analysis plan development and maintenance