The fifth trans-Atlantic workshop orgnanised in february 2023 was attended by representatives from UNICOM, US and EU regulators, biopharmaceutical manufacturers and technology vendors. Meeting discussions focused on global IDMP Implementation […]
COUNTRY/Topic DATE VIDEO SLIDES IRELAND : Lesson learnt June 6 2022 Link Link SWEDEN : strategy, projectmanagement and developmentofIT-systems October 14 2022 Link Link ESTONIA : overview (demo) of the new IDMP compliant […]
The Swedish Medicinal Products Agency is leading the UNICOM work package dedicated to IDMP implementation within National Authorities competent for market authorisation. Sweden is currently ensuring the Presidency of the […]
The Norwegian Medicines Agency is very much aware of its role of interoperabilty enabler and has initiated in 2019 the SAFEST project which aims at the distribution of interoperable medicinal […]
Norway, Belgium, Greece, Italy, Finland and the USA collaborate with UNICOM to provide a limited (4 substances) but complete IDMP/FHIR data set.
The process consists in collecting Data “AS IS”, and doing a central standardization to EDQM, limited to the minimal attribute list (variables relevant for pilots) and limited to 4 single […]
It is celebration day today (Jan 25) in Amsterdam at EMA headquarters. UNICOM is very pleased to announce that EU-SRS (the European Substances Registration System) is operational at EMA. The […]