Online
18.04.16 - 21.04.16
This webinar will support industry in understanding the substance, product, organisational and referential (SPOR) data services and related impacts. The European Medicines Agency (EMA) is establishing these business services for the central management and supervision of data in each of the four SPOR areas to facilitate the implementation of the ISO standards for the identification of medicinal products (IDMP). Following a phased implementation, pharmaceutical companies will be required to submit data on medicines to EMA in accordance with these formats and terminologies.