EudraPharm

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EudraPharm

EudraPharm (pronounced: yoo-dra-farm) is a database that was established by the European Medicines Agency (EMA) to provide public access to information regarding all medicinal products authorized in the European Union (EU) and the European Economic Area (EEA).

Etymology

The term "EudraPharm" is derived from the acronym EUDRA, which stands for European Union Drug Regulatory Authorities, and "Pharm", a common abbreviation for pharmacy or pharmaceuticals.

Description

EudraPharm is part of the Eudra informatics system, which includes other databases such as EudraCT (Clinical Trials), EudraVigilance (Pharmacovigilance), and EudraGMDP (Good Manufacturing and Distribution Practice). The EudraPharm database provides information about the therapeutic use, pharmacological properties, and potential side effects of authorized medicinal products. It also includes data on the marketing authorization holders, and the status of the marketing authorization.

Related Terms

  • European Medicines Agency (EMA): The agency responsible for the scientific evaluation, supervision, and safety monitoring of medicines in the EU.
  • European Union (EU): A political and economic union of 27 member states that are located primarily in Europe.
  • European Economic Area (EEA): The area in which the Agreement on the EEA provides for the free movement of persons, goods, services, and capital within the European Single Market.
  • EudraCT: The European Clinical Trials Database.
  • EudraVigilance: The European system for managing and analyzing information on suspected adverse reactions to medicines.
  • EudraGMDP: The EU database for Good Manufacturing and Distribution Practice.

External links

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