The new EudraVigilance system and the electronic reporting of individual case safety reports (ICSRs) in the ISO/ICH E2B(R3) format: hands-on training course
EventCorporate
Polish is available via eTranslation, the European Commission's machine translation service.
Translate to Polish | Important information about machine translation
Data
- poniedziałek, 9 Październik 2017, Cały dzień
Położenie
- European Medicines Agency, Amsterdam, the Netherlands
This hands-on training course covers the functionalities of the new EudraVigilance web application (EVWEB). It includes practical examples for creating, sending and accessing ICSRs in the new International Organization for Standardization (ISO)/ the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) E2B(R3) format. It covers reporting principles in accordance with the guideline on good pharmacovigilance practices (GVP) Module VI “Management and reporting of adverse reactions to medicinal products” and explanations on how to comply with the EudraVigilance business rules and the EudraVigilance access policy. The new EudraVigilance system and enhanced functionalities will go live in November 2017.