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Extended EudraVigilance Medicinal Product
Dictionary (DEEMED) e-learning
Session 1.2: Registration with EudraVigilanceVersion 5.3An agency of the European UnionEudraVigilance registration (1)
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Who needs dictionary xevmpd e-learning?
01
The dictionary xevmpd e-learning is useful for individuals or organizations involved in the pharmacovigilance field who need to gather, organize, and update information related to medicinal products and their safety in a standardized format.
02
This includes pharmacovigilance professionals, regulatory authorities, pharmaceutical companies, and other stakeholders who require a comprehensive and up-to-date dictionary for reporting and monitoring adverse drug reactions.
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What is dictionary xevmpd e-learning?
Dictionary xevmpd e-learning is a standardized dictionary used for coding adverse event information in pharmacovigilance.
Who is required to file dictionary xevmpd e-learning?
Healthcare professionals, pharmaceutical companies, and regulatory authorities may be required to use dictionary xevmpd e-learning.
How to fill out dictionary xevmpd e-learning?
Dictionary xevmpd e-learning is filled out by selecting the appropriate codes for adverse events based on standardized terminology provided in the dictionary.
What is the purpose of dictionary xevmpd e-learning?
The purpose of dictionary xevmpd e-learning is to ensure consistency and standardization in reporting and analyzing adverse events related to medications.
What information must be reported on dictionary xevmpd e-learning?
On dictionary xevmpd e-learning, information such as the type of adverse event, its severity, and any related medications or medical conditions must be reported.
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