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Elsevier's PharmaPendium(TM) Adds European Medicines Agency (EMEA) Documents
Date:10/14/2008

tant dimension to our coverage," said MacLaughlin. "This information will benefit companies operating globally because it provides critical access to another major regulatory body's points of view, precedents and data, including drugs approved only in Europe, and the availability of this information, combined with the FDA documents and other PharmaPendium data sources, will lead to a deeper understanding of the full scope of projected risks early in the drug development process and consequently reduce drug development costs and avoid regulatory cycling."

The EMEA Documents database is included as part of PharmaPendium licensing agreements at no additional fee and the content is automatically available to all users. More information about the European Medicines Agency and EMEA approval documents can be found at http://www.info.pharmapendium.com/emea.

About PharmaPendium(TM)

PharmaPendium (http://www.info.pharmapendium.com), The Essential Resource for Preclinical Safety and Risk Assessment, is a unique online resource that provides access via a single point to searchable and trusted drug information. It covers over 3100 approved drugs, with integrated preclinical, clinical and post-marketing safety data.

PharmaPendium is designed to meet the needs of preclinical safety assessment teams, toxicologists, pharmacokineticists, safety pharmacologists, regulatory affairs staff, pharmacoepidemiologists, clinical researchers and information specialists. It enables text-search of FDA Approval Packages and European Medicines Agency (EMEA) European Public Assessment Reports (EPAR) Approval Documents as well as other data sources. Adverse events and toxicity data are carefully extracted from preclinical and clinical studies from all of these sources. Elsevier offers a broad spectrum of solutions to make processes in drug disco
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SOURCE Elsevier
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