Identify best sites and most appropriate patients. Support protocol design.
- Protocol Design & Feasibility
- 正在进行的协议调整
- 利用RWD进行研究比较部门
- 优化国家分配
- 现场和患者选择
Finding the right information for your study is critical but can be overwhelming and tedious. IQVIA makes it easier by bringing a combination of unparalleled clinically-rich data, advanced analytics and human knowledge throughout the clinical development pathway. Studies can start sooner. Drugs can get to market faster. Safety can be firmly established. All while privacy is protected.
现实世界的数据可用于从开发到商业化后整个药物开发生命周期的许多不同目标。该数据可能与通过更有效的部位和患者认同来优化临床试验,了解疾病景观,丰富市场获取环境,后续的长期安全和药物利用模式以及支持商业分析。
One data source may not fully answer a question, therefore a combination or enrichment of data assets may need to be envisaged.
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