PharmaPendium 支持药物安全性和有效性决策，以获得更好的药物结果

为了推进最佳候选药物，您需要证明更好的性能。PharmaPendium 具有用户友好的工具，可帮助您分析安全性、可交付性和疗效数据。

• 自信地预测药物间相互作用

• 预测脱靶药物不良反应的风险（安全裕度）

• 通过跨临床前、临床和上市后的转化视图访问数据，包括：

  • 临床前和临床安全性

  • 动物模型

  • 不良事件 （MedDRA）

  • 药代动力学参数

  • 代谢和运输

  • 临床试验和终点

  • 盘后报告 （FAERS）

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Minimize regulatory cycling and avoid failing approval with PharmaPendium.

• Discover complete regulatory packages from the EMA and FDA, and FDA Advisory Committee Meeting Documents

• Explore previous regulatory submissions and learn from precedents to predict agencies’ requirements

• Benchmark against approved and withdrawn drugs with the same mechanism of action as your drug candidates

• Rapidly respond to regulatory questions using comparative data from FDA/EMA drug approval and review documents

Developed in collaboration with Pfizer, Tox Navigator includes toxicity data from regulatory documents and scientific articles.

Supporting the 3Rs and patient safety assessment, the Tox Navigator helps you:

• Convert animal doses to human equivalent doses (HEDs)

• Leverage existing data to reduce number of animal studies and design more efficient studies

• Investigate adverse drug reactions across different species

• Integrate in silico models and other non-animal testing methods

• Optimize research efforts by focusing on candidates with favorable safety profiles

Advance your research with Elsevier’s PharmaPendium and a portfolio of solutions for pharmaceutical R&D.

Innovate with confidence, supported by:

• Trusted quality information from regulatory data to peer-reviewed scientific literature

• Innovative technology that powers data transformation, and analytical and predictive tools

• Domain and data science expertise to solve complex problems with data solutions for R&D

Information integrity is essential to your progress. Discover trusted data and tools that deliver critical insights.

Let's shape progress together.