Vertaling van "data requirements " (Nederlands → Frans) :

Daarnaast werkte het Agentschap mee aan de ontwikkeling van een richtlijn over vaccins tegen mond- en klauwzeer: Draft reflection paper on data requirements for swine influenza vaccines against pandemic (H1N1) 2009 influenza en Guideline on data requirements for multi-strain dossiers for Inactivated vaccines against Avian Influenza, Blue Tongue and Foot and Mouth Disease.
L’Agence collabore également au développement d’une directive relative aux vaccins contre la fièvre aphteuse : Draft reflection paper on data requirements for swine influenza vaccines against pandemic (H1N1) 2009 influenza en Guideline on data requirements for multi-strain dossiers for Inactivated vaccines against Avian Influenza, Blue Tongue and Foot and Mouth Disease.

Speerpunt VACCINS voor diergeneeskundig gebruik. In 2010 was er een actieve deelname van het FAGG aan de werkgroep voor de evaluatie van immunologische producten en aan het CVMP in de ontwikkeling van drie belangrijke documenten met betrekking tot vaccins voor diergeneeskundig gebruik: -- Draft reflection paper on data requirements
Domaine d’excellence VACCINS à usage vétérinaire. En 2010, l’AFMPS a également activement collaboré au groupe de travail pour l’évaluation de produits immunologiques ainsi qu’au CVMP lors du développement de trois documents importants relatifs aux vaccins à usage vétérinaire : -- Draft reflection paper on data requirements

haemovigilance data and monitoring their implementation ●● The first annual report of the Haemovigilance Centre was published in 2007 Since November 2005, hospitals and blood establishments have been required to report to the Belgian Centre for Haemovigilance of the FAMHP serious reactions during the collection or administration of blood components and serious events relating to the quality or safety of blood components.
haemovigilance data and monitoring their implementation ●● The first annual report of the Haemovigilance Centre was published in 2007 Since November 2005, hospitals and blood establishments have been required to report to the Belgian Centre for Haemovigilance of the FAMHP serious reactions during the collection or administration of blood components and serious events relating to the quality or safety of blood components.