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Elsevier
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PharmaPendium 支援藥物安全性和有效性決策,以獲得更好的藥物結果

您需要高質量的數據來充滿信心地發現、創新和開發。PharmaPendium 將無與倫比的監管和藥物數據與全文搜索和預測工具相結合。使用 PharmaPendium 減少動物試驗並更快地推出藥物。

Women in white lab coats looking at computer screen

被 FDA 和世界頂級製藥公司使用

Get critical insights to predict the success or failure of drug candidates as early as possible

Video overview of PharmaPendium

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To advance the best drug candidates, you want to prove better performance. PharmaPendium has user-friendly tools to help you analyze safety, deliverability and efficacy data.

  • Predict drug-drug interactions with confidence

  • Predict the risk of off-target adverse drug reactions (safety margin)

  • Access data with a translational view across preclinical, clinical and post-market, including:

    • Preclinical and clinical safety

    • Animal models

    • Adverse events (MedDRA)

    • Pharmacokinetic parameters

    • Metabolism and transport

    • Clinical trial and endpoints

    • Post-market reports (FAERS)

Watch an introductory video

Make informed decisions to increase the success of regulatory submissions

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  • Benchmark against approved and withdrawn drugs with the same mechanism of action as your drug candidates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

Analyze the toxicity of drug candidates and advance the 3Rs with the new Tox Navigator

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

  • 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

Connected, configurable solutions to innovate in R&D

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.

Find precise data to advance your drug portfolio

DDI risk calculator picto

FDA 和 EMA 檔

利用 PharmaPendium 的強大功能,提供完整的 FDA 和 EMA 批准包以及重要的 FDA 諮詢委員會會議檔,這是其他工具所無法比擬的。
Efficacy data picto

Enhanced visualization

Seamlessly move from table view to interactive charts, graphs and visual aids to easily interrogate and interpret data.
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Predictive tools

Predict harmful DDIs using the DDI Risk Calculator and the risk of off-target adverse events using the Safety Margin Tool.
Cultivate curiosity picto

無與倫比的搜索功能

使用標準化數據按不良事件 (MedDRA)、靶點、適應症、藥物和終點查找資訊。結果頁面彌合了臨床前和臨床的鴻溝。
Reference picto

來自FAERS的真實世界證據

在FAERS(FDA不良事件報告系統)中搜索超過1900萬份報告,從真實世界證據和上市後藥物安全性中查找任何不良事件。
Data management picto

高品質數據集

PharmaPendium 的高品質數據集可供平臺外使用。將數據嵌入到您的工作流程和模型中,以實現更準確的搜索和預測。

"... PharmaPendium excels in retrieving specific toxicity observations across approval documents categorized by drug and species."

Guy Bouvier

GB

Guy Bouvier, PhD, ERT

Groupe Pierre Fabre 的 Director, Toxicology & Product Safety

Frequently asked questions

PharmaPendium Support Center

Get user-friendly tools to help you analyze drug safety, deliverability and efficacy data

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