Learning from each other: The UNICOM NCAs knowledge exchange workshops have been launched!
Twelve National Competent Authorities for medicinal products are actively involved in the UNICOM project. They are pioneering the implementation of the identification of medicinal products (IDMP) in the European Medicines Regulatory Network (EU MRN). Implementing IDMP standards in this […]
Community of Expertise webinar upcoming on Friday, 2 October, 15-16 CET: “UNICOM – Gap Analysis about existing and new standards and profiles”
The bimonthly “Community of Expertise” interactive sessions are organised by UNICOM work package 1 “IDMP-related standards and terminologies.” The webinars discuss current IDMP topics and further issues related to the […]
Webinar (21 Sept, 14:00 CET): Towards European data spaces for medicines – Semantic interoperability for patient safety
UNICOM contributes to the webinar: Towards European data spaces for medicines – Semantic interoperability for patient safety, that is being organised Monday, 21 September 2020, 14:00 – 15:30 CET. The […]
First reference documents of the EU-SRS – the European Substance Registration System are now available!
Background EU-SRS A team of experts from the European medicines regulatory network (European Medicines Agency and national medicines authorities from the EU Member States), supported by experts from the US […]
How to determine and manage a globally unique identifier for pharmaceutical products?
Next UNICOM Community of Expertise webinar upcoming on Friday, 4 September, 15-16 CET: How to determine and manage a globally unique identifier for pharmaceutical products? The UNICOM bimonthly interactive sessions […]
Upcoming Webinar “How to determine and manage a globally unique identifier for pharmaceutical products?” on Friday 4 September, 3-4 pm CEST
Next UNICOM Community of Expertise webinar upcoming on Friday, 4 September, 15-16 CET: How to determine and manage a globally unique identifier for pharmaceutical products? The UNICOM bimonthly interactive sessions […]