The EMEA has prepared this special EudraVigilance Medicinal Product Dictionary (EVMPD) course in the light of the implementation of the EU Directive on Clinical Trials (Directive 2001/20/EC).
This EVMPD course is addressing specifically all aspects related to the regulatory background, the definitions and procedures and the technical specifications for the handling and maintenance of IMP data and authorised medicinal product data in the EVMPD by the Sponsor or the MAH.
Participants will receive a training certificate that will allow them to register with EudraVigilance and to enter and maintain IMP and authorized medicinal product data in the EVMPD.
This EVMPD course is addressing specifically all aspects related to the regulatory background, the definitions and procedures and the technical specifications for the handling and maintenance of IMP data and authorised medicinal product data in the EVMPD by the Sponsor or the MAH.
Participants will receive a training certificate that will allow them to register with EudraVigilance and to enter and maintain IMP and authorized medicinal product data in the EVMPD.
