UNICOM – EMA Implementation Guide v2.0 The course of IDMP implementation in Europe is strongly influenced by European Medicines Agency's (EMA) guidance. On Monday 22 February, EMA released version 2.0 of […]
Understand the issues at stake and make your voice heard by attending the first UNICOM event targeted at national and European healthcare professionals and patients' organisations Download PDF Register NOW
The importance of medicinal product dictionaries (MPDs) is highlighted by two concrete examples. MPDs bring together the information on medicinal products from NCA and a variety of sources. Making sure […]
UNICOM – Representation of clinical information related to medication using SNOMED CT and other standards This webinar will illustrate the use of SNOMED CT and other standards for the representation and use of clinical information in […]
Initial roundtable discussion of groups involved in Adverse Events hosted by the FHIR Clinical Research Accelerator "Vulcan". Representatives from UNICOM T8.4 will "sit at the (round)table".
The meeting will update US key decision makers on the objectives and current achievements of UNCIOM and will open the way to to wider and more focused discussions on alignement […]
Register here: https://connectathon.ihe-europe.net/connectathon/ihe-europe-experience
The UNICOM Innovation Action has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 875299.
