The EMA database on PharmaPendium makes readily accessible approximately 140,000 pages of searchable documents for more than 300 active ingredients approved for the European market, some not approved in the US. It also presents preclinical and clinical toxicity and adverse effects data manually extracted from these documents. General product information documents are also included. EMA is the European agency for the evaluation of medicinal products. This new content offers critical insights into the EMA regulatory point of view, their reasoning underlying drug approval and the qualifications put on that approval.

European Medicines Agency's (EMA) European Public Assessment Reports (EPARs) - 80,000* pages of searchable EPAR documents on EMA-approved drugs, including over 50 drugs/mixtures not approved by the FDA. The EMA's EPAR documents cover medicines assessed by the Committee for Medicinal Products for Human Use (CHMP). EPAR documents include efficacy, indication, safety and pharmacokinetics data and mode of action information.

*See content updates for the most recent numbers.