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10 Feb 2011

EMA Launches New Version of EudraGMP

The European Medicines Agency has launched a new version of its EudraGMP database with information on manufacturing inspections.

The European Medicines Agency has updated its EudraGMP database giving the general public access to information on manufacturing inspections performed by regulatory authorities from all European Economic Area (EEA) countries.

 

EudraGMP, which was first launched in May 2007, contains information on all manufacturers of human and veterinary medicines located in the EEA, and other manufacturers outside the EEA that have been inspected by European regulatory authorities. It includes details of the manufacturers' manufacturing and importation authorisations and good-manufacturing-practice (GMP) certificates.

 

The latest version of the database allows public access to the authorisation and GMP certificates coming from all countri

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