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Early Development
我们的早期临床开发解决方案可在从候选化合物选择到第一阶段的每个阶段提供专家支持。
Regulatory Affairs Consulting
提供策略指导和端到端支持,以引导全球监管途径,确保药物开发从临床前阶段到整个过程高效、合规。
Pharmacometrics Services
我们经验丰富的定量药理学服务团队可帮助量化药物与患者之间的相互作用,优化开发和监管选择。
Quantitative Systems Pharmacology
选择 Certara 定量系统药理学 (QSP) 咨询服务,利用计算建模和实验数据加强药物开发。
Clinical Pharmacology
分析和策略,其主要目的是确保实现成功的药物开发计划。
Simcyp PBPK
将 PBPK 建模应用于药物开发各个阶段的全球咨询团队。
Biostatistics and Statistical Programming
高级生物统计咨询和符合 CDISC 标准的 SDTM 和 ADaM 数据集。
Regulatory Writing
我们的法规撰写服务为药物开发提供专业撰写的高质量文档,确保合规性和及时提交。
Real World Data Solutions
了解 Certara 全面的真实世界证据服务。我们为制药业提供创新的 RWE 解决方案,加强监管、市场准入和临床策略。

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