Local contact person for PV, including deputy and/or back-up PV person
02
Quality Control of translations and transcription for safety-related information
03
AE Processing - Case intake and follow-up
04
PV Training
05
PV Intelligence
06
Product Safety Information from Literature
07
Monthly Reconciliation
08
PSMF Updates
09
RMP and RMM
10
Vendor management
11
Report into EudraVigilance Database
12
Submit and retrieve medicinal product data using the extended EudraVigilance medicinal product dictionary (XEVMPD), the Article 57 database. This is aimed at ensuring the quality of data in the XEVMPD on authorized or investigational medicinal products.
