EUDRAEuropean Union Drug Regulatory Authorities
References in periodicals archive ?
5) The EU directive stipulated the creation of an EU-wide database, later called EUDRA CT, in which clinical trials conducted in the EU had to be registered.
EUDRA Volume 4, Annex 1, Manufacture of Sterile Products
EUDRA Volume 4, Annex 2, Manufacture of Biological Medicinal Products for Human use