Elsevier Information Solutions for Industry -- Products

PharmaPendium
QUICKFACTS

Only integrated and text-searchable source of FDA (back to first approved drug) and EMA documents
Covers over 4,000 approved drugs, with integrated preclinical, clinical and postmarketing safety data
Advanced functionality to compile and view drug information by adverse effect / toxicity, drug class, target and chemical structure
Thesaurus based on MedDRA

PharmaPendium USERS:

Toxicologists
Project Managers, Project Leaders
Pharmacokineticists
Safety Pharmacologists
Regulatory Affairs Staff
Pharmacoepidemiologists
Clinical Researchers
Medical Writers
Medical Officers
Information specialists/librarians

PharmaPendium is an invaluable source for anyone involved in drug development.
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How does PharmaPendium Work?
Download our quick start guide

"There are databases that are good to use and databases which are essential for my tasks. I think PharmaPendium is the latter. I would not be able to do the job without PharmaPendium…this database might affect a drug’s life or death. So, the value of this database cannot be evaluated according to 'how many users' or 'how often'."
Information Specialist,
Global Pharmaceutical Company

The definitive source of best-in-class drug information PharmaPendium is designed to help pharmaceutical professionals throughout a drug candidate’s life cycle with unprecedented access to Safety, Efficacy and Delivery data. It empowers users to reduce drug development costs by identifying and assessing risks earlier and drawing on historic precedent to avoid regulatory cycling.

With PharmaPendium you can search through more than 1,200,000 pages of FDA Approval Packages and 100,000 pages of searchable EPAR documents on EMA-approved drugs. PharmaPendium includes more than 4,000 approved drugs, with integrated preclinical, clinical and postmarketing safety data.

To learn more about PharmaPendium and how it can benefit your company visit our product website at
www.pharmapendium.com
www.info.pharmapendium.com