by Ursula Tschorn | Feb 17, 2017 | ISO IDMP Standards
RMS & OMS Mapping – Impact to Industry Concerning SPOR Data Mapping Activities the Industry is invited to start now with mapping activities. At the same time be aware, that the RMS and OMS lists are still worked on. The preparing activities are: SPOR...
by Ursula Tschorn | Nov 6, 2016 | Allgemein, News
Dosing IDMP1 Joint Venture The Dosing IDMP1 Joint Venture is building the Bridge from IDMP to E-Health. The supply of medicines to the population is a particular challenge worldwide: there are countless medicines and active ingredients that can develop unpredictable...
by Ursula Tschorn | Sep 28, 2016 | Clinical Trials
The EU clinical trial portal database The European Union (EU) clinical trial portal database will support a coordinated approach to clinical trial authorisation and supervision via a single application form for each clinical trial. The European Medicines Agency (EMA)...
by Ursula Tschorn | Sep 15, 2016 | Abbreviations
H+V is here meant to be the short form of Human and Veterinary domains.
by Ursula Tschorn | Sep 15, 2016 | Abbreviations
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...
