The UNICOM trans-Atlantic meetings are coordinated by CTADHL, a UNICOM partner formally tasked for trans-Atlantic outreach by UNICOM to include promotion and adoption of ISO IDMP across the medicinal product lifecycle. Although UNICOM is an EU initiative, it strongly considers collaboration and exchange with North American stakeholders as part of its remit to actively promote […]
Take part today at 13.00 in the 5TH ePI Vulcan accelerator discussion with a joint input of both UNICOM - Up-scaling the global univocal identification of medicines and Gravitate Health -> All the detailed information about the track can be found here: https://lnkd.in/eD8x3TQu This is the 5th event in the series of companion events to Vulcan ePI Project […]
Description: The landscape of use of medication data is quite broad and diverse. When looking at standards for the exchange of medication data, including the terminology mappings needed to cross the borders between the different domains, it is important to identify the original sources of the data being exchanged. These sources are the key first […]
This event is a webinar for industry and national competent authorities’ stakeholders wishing to learn more about data migration activities from SIAMED and xEVMPD databases to PMS
UNICOM is happy to announce a new series of IDMP implementation related training and knowledge transfer webinars in 2023. Considering the recent progress with EMA eAF we believe that it is important that all European NCAs acquire without delay a better understanding of the FHIR standard and its relevance in relationship to a wide IDMP […]
HL7 FHIR® is the communication standard for exchanging healthcare data being adopted worldwide. Past announcements from the FDA and current developments by the European Union (EHDS, EMA) and important and strategic projects such as UNICOM and Gravitate Health all prioritize the IDMP suite of standards as global reference and FHIR as underlying data transmission standard. […]
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Agenda : 25’ Results of the FAMHP IDMP gap analysis: 1. EMA : deviations (more, less, different) versus ISO IDMP documents (of 2012 and 2017, whichever is more recent) 2. FAMHP MPM/DTS : differences with the EMA data model 3. FAMHP approach to narrow the gaps 10’ QUESTIONS 15’ SAM / ePrescription : dataflow from BE […]
►You can register for the relevant Webinar by selecting the link below: SPOR and XEVMPD Data Governance - 17 April, 10:00-12:00 CET - https://ema-europa.webex.com/weblink/register/r9ca0c1044ed05282d0fe236251c99a9c Service Desk for SPOR and XEVMPD - 17 April, 14:00-16:00 CET - https://ema-europa.webex.com/weblink/register/r1552802c0646096c101b5e62b25dfa5d Referentials Management Service (RMS) - 18 April, 10:00-12:00 CET - https://ema-europa.webex.com/weblink/register/r46516995ff51d5f4383d95f05cac8e38 Organisation Management Service (OMS) - 18 April, 14:00-16:00 - https://ema-europa.webex.com/weblink/register/r834ea26426a57529292e0dcffc96cb5a Substance Management […]
Description: Referring to the landscape of medicinal product data – from “research and development” to “utilisation and outcome assessments”- the vision is that the essential IDMP identifiers remain used and unchanged along that life cycle. This Community of Expertise (CoE) will provide opportunity : for industry to present their perspective and needs, with large international […]
The UNICOM Innovation Action has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 875299.
