![]() ![]() The information in the database is continually updated by European regulatory authorities: the Agency expects around 3,000 new certificates to be imported into EudraGMP every year. facilitate the sharing of information on the outcome of inspections in the EU with regulatory authorities elsewhere in the world.eliminate the need for industry to submit applications in paper form.aid the co-ordination of activities related to manufacturing authorisations and GMP certificates between regulatory agencies in different European countries.improve the sharing of information between regulators and industry.This initiative, which is part of the Agency's drive towards a greater level of openness and transparency, will: Previously, limited information coming from only some European countries was available to the public. ![]() The latest version of the database allows public access to the authorisation and GMP certificates coming from all countries in the EEA, including all European Union (EU) Member States plus Iceland, Liechtenstein and Norway. It includes details of the manufacturers' manufacturing and importation authorisations and good-manufacturing-practice (GMP) certificates. The European Medicines Agency has launched a new version of its EudraGMP database giving the general public access to information on manufacturing inspections performed by regulatory authorities from all European Economic Area (EEA) countries.ĮudraGMP, 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.
0 Comments
Leave a Reply. |
AuthorWrite something about yourself. No need to be fancy, just an overview. ArchivesCategories |