Date

Thursday, 24 September 2020

Location

Online
European Medicines Agency, Amsterdam, the Netherlands

Event summary

This training session covers the registration process that needs to be completed before applicants can access the IRIS platform to submit their applications for certain EMA regulatory procedures.

The second part of this training is dedicated to research product identifiers (RPI), including why and when applicants require to use them in their scientific procedures applications to EMA.

    Video recording

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