| Author (Corporate) | European Medicines Agency |
|---|---|
| Publisher | EC |
| Publication Date | 2009 |
| Content Type | Overview |
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The EudraGMP database was initially launched in April 2007 in order to facilitate the exchange of information on compliance with good manufacturing practice (GMP) among the EEA national competent authorities (NCAs). The database contains information on all pharmaceutical manufacturers located in the EEA (EU Member States, Iceland, Liechtenstein and Norway) and other manufacturers which have been inspected by the NCAs. It includes details of those manufacturers' Manufacturing and Importation Authorisations and GMP Certificates. Version 2.0 of the database, launched in August 2009, will also contain Non-Compliance Statements. The information contained in the EudraGMP database will be completed and updated on an ongoing basis by the national competent authorities. For some national competent authorities, the publicly available information in the database is limited at the time of compiling this record. Public access will be phased in from 30 July 2009 onwards, as individual national authorities become ready. The deadline for public access to data from all national authorities will be January 2011. |
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| Source Link | Link to Main Source http://eudragmp.emea.europa.eu/inspections/displayWelcome.do |
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| Subject Categories | Business and Industry, Health |
| Countries / Regions | Europe |
