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Ema.europa.eu/ema/index. jsp curl pages/regulation/general/generalcontent000686. jsp COURSE DATES 23-25 January 2017 17500 27 February -1 March 2017 17502 24-26 April 2017 17506 15-17 May 2017 17507 pharmacovigilance in the EEA. EudraVigilance Training on Electronic Reporting of ICSRs in the EEA Duration 3 days Location European Medicines Agency EMA 30 Churchill Place Canary Wharf E14 5EU London UK OVERVIEW evaluation of Individual Case Safety Reports ICSRs related to all medicinal products...

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Step 1: Log in to the Eudravigilance training platform using your credentials

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Step 2: Navigate to the 'Training' section

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Step 3: Select the 'Eudravigilance Training on Electronic' course

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Step 5: Complete each module and pass any required assessments or quizzes

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Step 6: Once you have completed all the training modules, submit your completion certificate to the appropriate authority

Who needs eudravigilance training on electronic?

01

Pharmacovigilance professionals who work with electronic reporting systems

02

Drug safety officers and regulatory personnel involved in pharmacovigilance

03

Healthcare professionals who handle adverse drug reaction reporting

04

Anyone involved in the collection, evaluation, and reporting of drug safety data

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What is eudravigilance training on electronic?

EudraVigilance training on electronic is a training program that educates individuals on how to use the EudraVigilance system electronically to report and manage suspected adverse reactions to medicines.

Who is required to file eudravigilance training on electronic?

All individuals involved in the reporting and management of suspected adverse reactions to medicines are required to complete EudraVigilance training on electronic.

How to fill out eudravigilance training on electronic?

EudraVigilance training on electronic can be filled out online through the EudraVigilance system. Users must follow the guidelines provided in the training program.

What is the purpose of eudravigilance training on electronic?

The purpose of EudraVigilance training on electronic is to ensure that individuals have the necessary knowledge and skills to use the EudraVigilance system effectively and report suspected adverse reactions to medicines.

What information must be reported on eudravigilance training on electronic?

Information such as the suspected adverse reaction, the medicine involved, patient information, and relevant medical history must be reported on EudraVigilance training on electronic.

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