Pharmacovigilance

From CypDIS Online Help

Jump to: navigation, search

The system aims to collect, process and evaluation of adverse events occurring during the use of medicinal products for human use and extraction of useful conclusions and / or action.

Users system:
Users of the system are classified into two categories: 1. Health Professionals (external users) who are able through the Internet to electronically submit reports of adverse events (Yellow Card) and 2. Specialized personnel of Pharmaceutical Services, which may enter occurrence reports and to prepare the reports lodged.

Features:

  • Case management with tracking of correspondence and action (follow ups, etc.)
  • Export reports to a file format XML, structured along the lines of EudraVigilance
  • Find references with multiple criteria (eg time limits)
  • Evaluation reports using the Navajo algorithm
Personal tools
Pharmacovigilance
BI Platform
Portal administration
Database