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PharmaPendium is the most powerful way to advance your drug portfolio

Used by the FDA and the world’s top pharma companies, PharmaPendium supports key decisions on drug safety and efficacy. Reduce animal testing and launch life-changing therapies faster with the unparalleled regulatory and drug data in PharmaPendium.

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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Benchmark against approved and withdrawn drugs with the same mechanism of action as your drug candidates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:
- Adverse effects
- Animal models
- Drug-drug interactions
- Clinical endpoints
- Safety margin

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."

GB

Guy Bouvier, PhD, ERT

Groupe Pierre Fabre의 Director, Toxicology & Product Safety

Frequently asked questions

PharmaPendium Support Center

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

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관련 링크

PharmaPendium Support Center