A B C D E G H I L M N O P R S T U X
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eSubscription in Europe and US

by | May 22, 2015

eSubscription is the process of registering medicinal products for marketing authorisation at the local authorities. eSubscription requires in current regulations in the US and Europe substantially different technologies, terminologies and vocabularies for...

EU IDMP Task Force

by | Jul 5, 2015

The EMA and the EU Regulatory Network have founded an EU IDMP Task Force with the involvement of terminology organisations, software vendors and developers of medicinal products dictionaries or databases. The task force will be responsible for advising on the...

EUNDB

by | Jul 31, 2015

The European Union Network Data Board (EUNDB) is an advisory body co-chaired by the Head of Business Data and Support Department of the EMA.

EUTCT

by | Sep 15, 2016

EUTCT is a central repository and publication system for controlled term lists used in the European medicines regulatory network. It is a repository and provider of controlled terms (or controlled vocabularies) in multiple languages. It is the predecessor of RMS. RMS...