Whatever your role in the drug development and approval process, PharmaPendium can help.

PharmaPendium provides powerful decision support by giving you unprecedented access to best-in-class drug development information.

The only online resource to hold FDA approval documentation since 1938, as well as valuable EMA EPARs, PharmaPendium gives you unrivalled insights into the entire history of drug development. 

PharmaPendium offers:

• Searchable FDA and EMA approval packages.
• The PharmaPendium Classic collection, containing archived FDA approval documentation from 1938 – 1992.
• Carefully extracted adverse event and toxicity data from preclinical and clinical studies, as well as a database of post market event reports – allowing you to view which studies’ results translate successfully from animal to human, or from clinical to post-marketing.
• Data search function by text or chemical structures or data pathway browsing by drug, adverse event/toxicity and target.

Helping you to:

• Quickly find the information you need – without having to order relevant packages and scan through printed documents.
• Easily generate, retrieve and compare information.
• Reduce the risk of submission mistakes with access to critical insights into the FDA and EMA approval precedents, highlighting where previous submissions have succeeded or been delayed.
• Reduce development costs by learning from approved drugs and identifying drug safety risks earlier.

Who uses PharmaPendium?

PharmaPendium is an invaluable resource for all those involved in drug development.

From the discovery, preclinical through to clinical and post-marketing phases, PharmaPendium’s unique ability to facilitate the faster retrieval of comparative exposure data and regulatory precedents helps significantly improve workflows for multiple departments:

• Safety Assessment including:
  • Toxicologists
  • Safety Pharmacologists
  • Project Leaders
• Pharmacokineticists
• Regulatory Affairs
• Medical Officers & Clinical Writers
• Discovery
• Pharmacoepidemiologists
• Information Managers

Whether you’re involved at the Preclinical or Clinical stage, in Drug Safety, Pharmacokinetics, Regulatory Affairs or Information Management, PharmaPendium is the only drug development resource to provide you with the data you need in a scientific, regulatory and commercial context.