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PharmaPendium is the most powerful way to advance your drug portfolio

Find the best strategy for your drug candidates’ safety and efficacy. Reduce animal testing. Go to market faster with safer life-transforming treatments for patients. Trusted by the FDA, PMDA and the world’s top 20 pharma companies.

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Predict success or failure of candidates for your drug portfolio as early as possible

  • Find powerful preclinical and clinical data and tools for the translation to humans

  • Benchmark against approved and withdrawn drugs with the same mechanism of action as your drug candidates

  • Predict:

The more you find and predict, the less animal testing you need.

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Successful regulatory submissions

  • Predict fast and effective strategies for the success of all regulatory submissions

  • Use PharmaPendium to minimize regulatory cycling and avoid failing approval

  • Find information about previous regulatory submissions and profit from precedents to predict agencies’ requirements

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Find precise data — like in no other tool

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FDA and EMA documents

Harness the power of PharmaPendium with complete FDA and EMA approval packages and critical FDA Advisory Committee Meeting documents, like in no other tool.
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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.
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Unparalleled search capabilities

Find information by adverse events (MedDRA), targets, indications, drugs and endpoints using normalized data. Result pages bridge the preclinical to clinical divide.
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Real-world evidence from FAERS

Search over 19 million reports in FAERS (FDA Adverse Event Reporting System) to find any adverse event from real-world evidence and post-market drug safety.
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Machine-readable data

PharmaPendium’s high-quality datasets are available for off-platform usage. Embed the data into your workflows and models for more accurate search and prediction.

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

Guy Bouvier


Guy Bouvier, PhD, ERT

Director, Toxicology & Product Safety at Groupe Pierre Fabre

Frequently asked questions

The most powerful way to advance your drug portfolio | PharmaPendium. Find it. Predict it.

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