Menu Back toMandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting in the EU: Virtual Training Course using the EudraVigilance System

Mandatory use of ISO/ICH E2B(R3) Individual Case Safety Reporting in the EU: Virtual Training Course using the EudraVigilance System

Virtual live training course including EMA required knowledge evaluation, on how to report, view and download ICSRs using the EudraVigilance system and principles of EVDAS.


Overview

The European Medicines Agency (EMA) launched the enhanced EudraVigilance system in November 2017, which supports reporting and analysis of suspected adverse reactions originating from clinical trials and the post-authorisation phase of medicinal products. 

Based on a  Pharmacovigilance Risk Assessment Committee (PRAC) recommendation, the EMA Management Board confirmed and announced the mandatory use of the ISO Individual Case Safety Report (ICSR) standard based on the ICH E2B(R3)[1] modalities as of 30 June 2022 for all reporting to EudraVigilance.

Furthermore, the ISO standard terminology for pharmaceutical forms and route of administration will also become mandatory at the same time. The use of the ICH E2B (R2) format will therefore be phased out.

The training course includes a knowledge evaluation for which participants, who pass the evaluation, will receive a notification from the EMA. Organisations, which aim to use EudraVigilance web application (EVWEB) to start the electronic reporting of ICSRs to Eudravigilance for the first time, need to provide such notification for at least one user to be able to successfully register with the EudraVigilance production environment. 

For more information on the registration process, please consult the EMA website

 [1] http://estri.ich.org/e2br3/index.htm

Who should attend?

Users of EudraVigilance – new users and users already trained on working with EudraVigilance including

  • Professionals of Marketing Authorisation Holders
  • Sponsors of a Clinical Trials
  • National Competent Authorities or those acting on their behalf, in charge of pharmacovigilance and drug safety with obligations to report suspected adverse reactions related to medicines

Participants are expected to work in pharmacovigilance and to have basic background knowledge of:

  • The EU pharmacovigilance legislation
  • GVP Module VI – Management and reporting of adverse reactions to medicinal products
  • Guidance documents related to the monitoring of safety of clinical trials (CT3)
  • GVP Module IX – Signal management and revised guidance on statistical methods

Further information on the new EudraVigilance system training can be found on the dedicated EMA EudraVigilance training page.

Learning objectives

By the end of this training course, participants should be able to:

  • Describe the EudraVigilance System components
  • Apply ISO/ICH E2B(R3) rules to safety reporting based on practical examples for initial and follow-up reports, amendment and nullification reports, literature and parent-child cases, and reports from studies
  • Understand how to use EVWEB to create, send and access ICSRs and acknowledgments
  • Describe the principles of EVDAS and access by MAHs to use electronic Reaction Monitoring Reports (e-RMRs), line listings and ICSR forms
  • Query, view, browse and download ICSRs using the EudraVigilance ICSR Download Functionality, which provides access by marketing authorisation holders (MAHs) to ICSRs submitted by national Competent Authorities (NCAs) in the EEA

Contact us



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+41 61 225 51 51


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