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REGISTRATION FORM The NEW EudraVigilance System and the electronic reporting of Cars in the ISO/ICH E2B(R3) format #19500 2426 June 2019 ONE Academy, Athens, Greece EMAIL YOUR COMPLETED REGISTRATION
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What is form new eudravigilance system?
The new EudraVigilance system is a system used for the electronic reporting of suspected adverse reactions during the development and marketing of medicines in the European Economic Area (EEA).
Who is required to file form new eudravigilance system?
Marketing authorization holders, sponsors of clinical trials, and healthcare professionals are required to file reports through the new EudraVigilance system.
How to fill out form new eudravigilance system?
To fill out the form in the new EudraVigilance system, users must log in to the system, select the appropriate reporting category, and enter the necessary information about the adverse reaction.
What is the purpose of form new eudravigilance system?
The purpose of the new EudraVigilance system is to facilitate the electronic reporting and monitoring of suspected adverse reactions to medicines, improving patient safety.
What information must be reported on form new eudravigilance system?
Information such as the suspected adverse reaction, the patient's details, the medicinal product involved, and the reporter's contact information must be reported on the form.
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