Skip to main content

Unfortunately we don't fully support your browser. If you have the option to, please upgrade to a newer version or use Mozilla Firefox, Microsoft Edge, Google Chrome, or Safari 14 or newer. If you are unable to, and need support, please send us your feedback.

Elsevier
Publish with us

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.

Business people in a meeting

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  • Benchmark against approved and withdrawn drugs with the same mechanism of action as your drug candidates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

Watch the videoopens in new tab/window

PharmaPendium product video

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

Business meeting within pharmaceutical industry

Find precise data — like in no other tool

DDI risk calculator picto

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.
Efficacy data picto

Enhanced visualization

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

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

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.
Reference picto

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.
Data management picto

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

GB

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.

Business people in meeting

Related links