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REGISTRATION FORM The NEW EudraVigilance System and the electronic reporting of Cars in the ISO/ICH E2B(R3) format #18577 2123 February 2017, ONE Academy, Athens, Greece EMAIL YOUR COMPLETED REGISTRATION
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Access the EudraVigilance system website.
02
Click on the 'Login' button and enter your credentials.
03
Navigate to the forms section and select the 'New form' option.
04
Fill out the required fields in the form, such as product information, adverse event details, and reporter details.
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Submit the form by clicking on the 'Submit' button.
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01
Pharmaceutical companies
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Healthcare professionals
03
Regulatory authorities
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What is form new eudravigilance system?
The Form New EudraVigilance System is a standardized document used for reporting adverse drug reactions and other safety-related data within the European Union.
Who is required to file form new eudravigilance system?
Pharmaceutical companies, healthcare professionals, and regulatory authorities are required to file the Form New EudraVigilance System.
How to fill out form new eudravigilance system?
The form can be filled out online via the EudraVigilance portal, ensuring all required fields are completed accurately with relevant data.
What is the purpose of form new eudravigilance system?
The purpose of the Form New EudraVigilance System is to enhance the monitoring of the safety and efficacy of medicines through timely reporting of adverse events.
What information must be reported on form new eudravigilance system?
The form must report information such as patient demographics, medication details, adverse event descriptions, and outcomes of the event.
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