EU: EMA reminds applicants on the mandatory use of EU M1 spec 1.4 for EU eCTDs

The European Medicines Agency EMA reminds all applicants that from 1 July 2010 the EU regional Module 1 v1.4 (see our related News Article) must be used for all eCTD submissions for all European procedures, and any eCTD submissions provided from this date using any previous version of the EU M1 specification (v1.0. v1.1, v1.2.1 or v1.3) will not be accepted.

[Source: EMA website]

<- Back to: eCTD News