We
understand that the EudraVigilance e-learning XEVMPD course will be
released "at the end of April at the latest". The EMA has confirmed
that "following a successful completion of the competency assessment,
users will receive an XEVMPD training certificate." This is good news, and will be a very welcome resource.
The current on-site courses offered by the EMA are aimed at facilitating the practical implementation of the requirements, including technical aspects and all related procedures on electronic submission of information on medicines by marketing authorisation holders in the European Union (EU). The two-day on-site training courses focus on explaining the guidance, specifically the mandatory data elements necessary for the electronic submission of information on medicinal products, and applying the format of the eXtended EudraVigilance Product Report Message (XEVPRM).
The current on-site courses offered by the EMA are aimed at facilitating the practical implementation of the requirements, including technical aspects and all related procedures on electronic submission of information on medicines by marketing authorisation holders in the European Union (EU). The two-day on-site training courses focus on explaining the guidance, specifically the mandatory data elements necessary for the electronic submission of information on medicinal products, and applying the format of the eXtended EudraVigilance Product Report Message (XEVPRM).
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