UNICOM supports the further development of the EU cross-border digital health services
Excellent attendance at the 1st UNICOM/eHDSI workshop dedicated to EU eHealth cross-border services More than 80 people attended a two-day workshop organized in February by UNICOM dedicated to the beneficial […]
EMA Implementation Guide v2.0 is released: Let’s analyse it together on the 23rd of March during our next “Community of Expertise” meeting!
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 its Implementation guide (EU IG […]
WHO Collaborating Centre for drug statistics methodology in Oslo formally agrees to collaborate with unicom
UNICOM has already welcomed the active involvement of the WHO Collaborating Centre UMC (Uppsala Monitoring Centre, Uppsala, Sweden) on questions related to the identification of substances in a pharmacovigilance context. UNICOM is now also delighted […]
Do not miss the next UNICOM Community of Expertise on Friday 19 February 2021 on the theme: UNICOM – IDMP Logical Model
The UNICOM project has compiled and published a set of requirements for a new IDMP logical model, which shall be technology independent. The presenters will share with you the content and […]
Share your opinion on the future of EU Digital Health Apps!
UNICOM invites you to participate in a survey of public opinions on what is important regarding patient care and empowerment when travelling outside one’s home country, specifically related to medicine. […]
The european substance reference system (EU – SRS) release strategy widely supported by the community
EU-SRS provides scientifically sound descriptions of substances used in medicinal products in the EU by applying regulatory standards for the identification of medicinal substances in accordance with the ISO IDMP standards. This is […]