Traduction de «reporting pharmacovigilance » (Néerlandais → Français) :

A simple guide for veterinary pharmacovigilance has been published on the FAMHP website; together with the associated reporting form this has also been sent to all veterinarians and pharmacists.
A simple guide for veterinary pharmacovigilance has been published on the FAMHP website; together with the associated reporting form this has also been sent to all veterinarians and pharmacists.

Currently priority is focused on the awareness campaigns for healthcare professionals which are intended to promote the utility and importance of reporting pharmacovigilance of medicines for human and veterinary use.
Currently priority is focused on the awareness campaigns for healthcare professionals which are intended to promote the utility and importance of reporting pharmacovigilance of medicines for human and veterinary use.

The initial results of the “Active pharmacovigilance” project have been very encouraging given that the number of reports received by the FAMHP has more or less doubled between 2007 and 2008.
The initial results of the “Active pharmacovigilance” project have been very encouraging given that the number of reports received by the FAMHP has more or less doubled between 2007 and 2008.

to pharmacovigilance and a European Organisation of 10 roadshows in Flanders, reporting form to veterinarians and retail 11 in Wallonia; a total audience of 1000 pharmacists; veterinarians was reached in this way.
to pharmacovigilance and a European Organisation of 10 roadshows in Flanders, reporting form to veterinarians and retail 11 in Wallonia; a total audience of 1000 pharmacists; veterinarians was reached in this way.

De vergunninghouder stelt zich verplicht om de onderzoeken en verdere maatregelen ten behoeve van de geneesmiddelenbewaking uit te voeren zoals uitgewerkt in het Pharmacovigilance Plan zoals overeengekomen in het RMP, opgenomen in module 1.8.2 van de handelsvergunning, en in enige daaropvolgende, door het Comité voor geneesmiddelen voor menselijk gebruik (CHMP) goedgekeurde herziening van het RMP. Conform de richtlijn van het CHMP met betrekking tot risicomanagementsystemen voor geneesmiddelen voor menselijk gebruik, moet de herziening van een RMP gelijktijdig met het eerstvolgende Periodic Safety Update Report (PSUR) worden ingediend.
Plan de gestion des risques (PGR) Le titulaire de l’autorisation de mise sur le marché réalisera les activités décrites dans le plan de pharmacovigilance comme convenu dans le PGR présenté dans le Module 1.8.2 de l'autorisation de mise sur le marché, ainsi que toutes actualisations ultérieures du PGR adoptées par le comité des médicaments à usage humain (CHMP).