by Ursula Tschorn | 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...
by Ursula Tschorn | 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.
by Ursula Tschorn | 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...