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 meeting belongs to the EHTEL “Imagining 2029” work programme. As a virtual meeting of the EHTEL/ELO Network it is part of its Moving Towards European Health […]
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 identification of medicinal products in regulatory and clinical contexts. The webinars are complemented by an extensive questions and comments section. The group of attendees is growing, […]
In February 2020, the European Commission unveiled its data strategy, culminating in the creation of an infrastructure and governance for the free flow of personal data under the control of individuals. Following this announcement, Digital New Deal has published Personal Data Sharing: Governance as a Game Changer. Governance is needed to enable the switch from […]
As one of the highlights of Germany’s Presidency of the Council of the EU, the High-Level Conference “Digital Health 2020 – EU on the Move” aims at advancing discussions in the area of digital health. Federal Minister of Health of Germany, Jens Spahn, will open the conference bringing together representatives from all parties involved in […]
The UNICOM monthly, interactive Community of Expertise webinar sessions address issues related to the identification of medicinal products (IDMP) in regulatory and clinical contexts. On Thursday November, 12th UNICOM holds the fourth CoE webinar addressing: How substances/products have been selected for piloting, and How this is moving to support use of IDMP data across multiple domains […]
The UNICOM monthly, interactive Community of Expertise webinar sessions address issues related to the identification of medicinal products (IDMP) in regulatory and clinical contexts. On Friday, 4 December, UNICOM holds the fifth CoE webinar addressing how IDMP is supporting COVID-19 immunization: A number of new vaccines will arrive on the market with the purpose to […]
How digitalisation can support the regulatory business process Britt Vermeij, Vice-Chair of the Regulatory and Scientific Affairs Committee Medicines for Europe, TEVA - A coherent data strategy as foundation to respond to public health needs Remco Munnik, Chair of the Telematics WG Medicines for Europe, Iperion - Open dialogue between industry and regulators: How digitalisation […]
UNICOM – Pharmaceutical Dose Forms The presenters will share their perspective on how the pharmaceutical dose forms have been developed and are currently used in different situations. They will give insight in the current revision of the ISO standard, which intends to provide easier means to define world wide unique pharmaceutical dose forms.
The objectives of this Workshop are to present in some detail the history, and particularly the present organisational structure, data flows and technical details of the ePrecription/eDispensation and Patient Summary healthcare services as provided in the context of the CEF eHDSI and to give a preliminary glimpse of the new requirements resulting from IDMP implementation […]
The objectives of this Workshop are to present in some detail the history, and particularly the present organisational structure, data flows and technical details of the ePrecription/eDispensation and Patient Summary healthcare services as provided in the context of the CEF eHDSI and to give a preliminary glimpse of the new requirements resulting from IDMP implementation […]
The UNICOM project has compiled and published a set of requirements for a new IDMP logical model, which shall be technology independent. Currently, the IDMP data model is described by partial logical models across the different standards making up the IDMP set of standards and by HL7 v3 based specifications in some of the technical specifications. The ISO group of experts will take these requirements as input for the development of a new ISO IDMP logical model. Our discussion of the requirements will also be made available to the ISO experts, as they join the conversation.
Joint Initiative Council Open Forum - Morning Session Transcending national boundaries and organizations, the Joint Initiative Council’s standards development organizations work collaboratively to provide global, coordinated—not competitive—standards that address real-world healthcare issues. In its recently released white paper, the JIC explores the desired future of a digital health ecosystem where high-quality data is available to […]
Transcending national boundaries and organizations, the Joint Initiative Council’s standards development organizations work collaboratively to provide global, coordinated—not competitive—standards that address real-world healthcare issues. In its recently released white paper, the JIC explores the desired future of a digital health ecosystem where high-quality data is available to the right people, at the right place and […]
The current status of UNICOM work and expected results is presented by C.Hay (WP1) at the meeting of the International pharmaceutical regulators programme (http://www.iprp.global/home)
Preliminary Program Welcome – Agenda State of play with Vaccination Standards in Europe: an overview Christof Gessner, HL7 Europe Board of Directors, HL7 Germany What is the state of play of implementations across Europe? Role of HL7 Standards? Role of Affiliates? collaborations – decision-making practices – vendor engagement? Vaccination Standardization Efforts across Europe (deep dive, […]
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 its Implementation guide (EU IG v2.0). This is a very important milestone for UNICOM and our communities, which will be presented and discussed at our […]
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 that the identification of the medicinal product across these sources can be done automatically and without error, makes the implementation of IDMP such a crucial […]
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 a select number of scenarios across the UNICOM landscape of IDMP implementation. The MHRA will demonstrate the use of SNOMED CT coded data in an actual electronic health […]
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 possibilities. The EU UNICOM Trans-Atlantic Stakeholders Webinar will be officially coordinated by *CTADHL, a UNICOM partner formally tasked for trans-Atlantic outreach by UNICOM to include […]
Register here: https://connectathon.ihe-europe.net/connectathon/ihe-europe-experience
IDMP in Europe - what does it mean for you? Presentation by Robert Stegwee Free registration at: https://connectathon.ihe-europe.net/experience-sessions-tuesday-15-june
UNICOM – Cross-border ePrescription - standards, terminologies, processes You will learn what UNICOM is expected to contribute in order to make this service truly operational and reliable: The implementation of IDMP across Europe provides important opportunities for the improvement of cross-border services, such as ePrescription. UNICOM is tasked with elaborating these opportunities into change proposals […]
What is the relation between INN, ATC and substance identification according to IDMP? For the identification of substances, IDMP relies on data available in the Global Substance Registration System (GSRS). Its European counterpart EU-SRS is being implemented, supported by UNICOM WP 2, where an important data cleansing work is in progress. This webinar will cover the […]
The presentations will focus on the background, purpose, and governance of each of these identification and classification systems as well as their linkage. The discussion will also address how their use outside the originally defined scope may have consequences and limitations for the correct use of medicinal products across the countries. Presenters: Dr Rafaella Balocco […]
A medicine’s ePI ( Electronic Product Information) is regulated, scientifically validated information to assist healthcare professionals in prescribing and dispensing, and informs patients and consumers about their medicine and its safe use. Thus, trusted access and understanding of up-to-date product information on medicines when and where it is needed is extremely important. In Europe, the […]
Defining characteristics for dose forms, which meet global needs, is a challenge addressed by EDQM and several stakeholders. This webinar will present the views regarding the “global” aspect of dose form definition: in the regulatory space, in the clinical space, in the domain of adverse event monitoring and what efforts EDQM is deploying to meet […]
Dear members of the UNICOM Consortium. You are cordially invited to the HL7 Europe Listening Session. The purpose of this session is to inform the HL7 International community of specific developments in European countries and Europe as a region. Short topical introductions will be provided by the Board Chair of HL7 International and some of HL7 […]
This year the 19th International Conference on Informatics, Management, and Technology in Healthcare (ICIMTH 2021) is announced as an eConference (no physical presence is required) due to the COVID-19 pandemic. The Conference (www.icimth.com) will be held for this year on: 16-17 October, 2021. The modification of the traditional Conference to a Virtual event is due to […]
The world is teaming up to provide clarity on the identification of substances and the representation of strength. This Community of Expertise will present different recent perspectives on these activities, with speakers reprensenting the views and work of regulatory, industry and standards stakeholders. Speakers: Isabel Chicharo, EMA: Implementing substance cleansing results in SMS Petra Kristic, […]
Scenarium in cooperation with Fundisa - African Academy of Medicine Development, supported by GHA-German Health Alliance as well as other prominent partners are organising the first edition of an international workshop on Health Economics and Pharmacoeconomics: Opportunities for German-African Cooperation October 30-31, 2021 hybrid event The workshop will take place simultaniously at University of Potsdam, […]
This is a closed event. We already had presentation from a number of partners and this time we kindly invite: - BfARM (DE) - ARMPS (BE) - INFARMED (PT) to present lessons learnt from their view. We also invite ALL partners to share experiencies during the discussion.
The UNICOM Trans-Atlantic meeting will be officially 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 […]
Topic: Using IDMP in Adverse Event reporting and Individual Case Safety Reports (ICSR) Date: 3 December between 3 – 4:30 pm CET Presenters: Anja van Haren Barry Hammond (UNICOM WP 1 and MedDRA) Sarah Vaughn (MHRA) Panelists: Julie James (UNICOM WP 9 and BlueWaves) Jane Millar ( UNICOM WP 1 and SNOMED CT)
This event is open to ALL National Competent Authoritities; If you have not received an invitation, send a request to the follwoing email adress: WP4 kindly invites you to the follow-up training based on the concept presentation we had last year. We will prepare a FHIR example. We will use EMA's LOSEC example as […]
The need for global identification of vaccines has been recognized in the Global Vaccines Initiative, addressing the global surveillance of vaccine effectiveness and risks. This has particular consequences for the European Substance Registration System, the focus of UNICOM WP 2, which will need to make sure that cleansing and building of substances is done in […]
The Digital Application Dataset Integration (DADI) project will replace PDF electronic application forms (eAF) used for regulatory submissions with online forms, making the future form-filling and submission-handling process more efficient. This first public webinar is for stakeholders from the human & veterinary medicines industry and national competent authorities wishing to learn more about the following: DADI roadmap […]
This second public webinar is for technical experts from industry and national competent authorities wishing to learn more about the design of the FHIR message for the first form to be updated: Human Variations. Despite the focus on human medicines, all stakeholders interested in the technical aspects of the FHIR message are welcome. Topics addressed in this webinar […]
All infos here
Workshop only upon invitation. If you have not received an invitation altjough you work with or for an NCA and would like to take par: send a mail to
All info available here: https://unicom-project.eu/discover-what-can-idmp-do-to-improve-the-quality-of-drugs-dictionaries-and-support-best-etl-practices-during-our-community-of-expertise-on-february-25-at-15-00-cet/
This webinar is an introduction to the Organisation Management Service (OMS) and Referentials Management Service (RMS) services and activities for industry users. The morning session, from 10:00 to 11:30, is dedicated to RMS: Introduction to RMS RMS processes: Data Stewardship (CRs, deltas ) and Service Desk RMS Statistics: CRs & SLAs, Service Desk & SLAs, Customer satisfaction […]
Date: 18/03/2022 Location: Online, 14:00 - 16:00 Amsterdam time (CEST) How to request access to SPOR API Where to find SPOR help and support SPOR API resources and concepts SPOR API demo SPOR API tips for better use/querying Registration
UNICOM will be present in the DIA event in the following sessions: Wednesday, March 30th, 13:15 - 14:15, Hall 100: link to the session Thursday, March 31st, 09:00 - 10:15, Hall 100: link to the session
Worshop upon invitation only. If you wish to attend, please send a request to The workshop objectives are the following ones: - Participants will be able to understand and read FHIR messages describing medicinal products; We will be using draft FHIR-messages provided by EMA/DADI - Seceral National Competent Authorities will also prepare examples which […]
During this third trans-Atlantic meeting we will have a focus on the adoption of the IDMP data model and related IDMP activities in the US. Additionally other global IDMP activities will be addressed. Welcome, introduction to CTADHL and UNICOM (Vada Perkins, Frits Stulp and Christian Hay) Main & Open discussion Introduction: US (Elaine Johanson, […]
IDMP implementation will be the central topic on April 6 but many other sessions will also have IDMP in the background. UNICOM will be represented in two sessions at 10.45 and 15.45 on April 6. All infos and agenda:
Semantic specifications for eHealth services This webinar will present a selection of requirements identified by UNICOM WP 5, detailed in its draft deliverable D5.4, "Semantic Specifications". Their purpose is to support semantic interoperability to be considered in local, national or regional specifications for electronic prescription, electronic dispensation and patient summaries. The requirements are a source […]
During the next HL7 VULCAN Accelerator, the focus will be on the FHIR specification set up by the European Medicines Agency on Electronic Product Information and more partcularly FHIR standard for Patient Information Leaflets of Medicines. More info: https://unicom-project.eu/join-the-unicom-and-gravitatehealth-for-the-next-epi-hl7-vulcan-accelerator-on-may-3-13-14-cest/
An UNICOM abstact has been accepted. UNICOM is thus proud that it will be part of the official programme with a full oral presentation. Lin to the event: https://mie2022.org/
Those webinars are meant to facilitate an early and detailed cross-fertlisation between European National Competent Authorities. Ireland (HPRA) will be presnting its current sttaus on its road toward IDMP implementation. All staff of all European agencies are warmly welcome to attend. If you have not received an invitation but would like to attend, please send […]
The Croatian Medicinal products and medical devices Agency (HALMED) will be presenting its roadmap to IDMP implemenation at this event. See: https://www.iaria.org/conferences2022/eTELEMED22.html
The Digital Application Dataset Integration (DADI) Network project team is pleased to announce the publication of the first version of the eAF Portal guide to registration. The guide aims to support the users of the eAF Portal in completing the registration steps before accessing the platform. Most of these steps are independent from the eAF Portal and […]
Advancing Pharmacoepidemiology and Real-World Evidence for the Global Community UNICOM WP8 leader Robert Vanderstichele will be presnting a poster on the the theme: Will the implementation of ISO/CEN Standards for global Identification of Medicinal Products (IDMP) make any difference for pharmaco-epidemiology ? Vander Stichele RH, Sturkenboom MCJM, Duran C, Nicolas L, Kalra D, Fladvad M.
The next UNICOM Community of Expertise is scheduled on Friday 26 August 2022: In collaboration with the Gravitate Health project and the Vulcan Accelerator ePI project, UNICOM has contributed to a track at the May HL7 FHIR Connectathon. The scenario being developed was on a travelling lady needing treatment to a recurring condition, for which […]
The Digital Application Dataset Integration (DADI) Network project team is pleased to announce the publication of the first version of the eAF Portal guide to registration. The guide aims to support the users of the eAF Portal in completing the registration steps before accessing the platform. Most of these steps are independent from the eAF Portal and […]
The purpose is to familiarize the UNICOM partners and impacted stakeholders with the well-established and robust IHE testing and certification process, including the tooling available to support these processes. The session will have a special focus on the interactions between Regulation and Authorization authorities - industry (representing Development and Production) and medicinal product dictionary providers […]
The International Pharmaceutical Federation (FIP) is the global body representing pharmacy and pharmaceutical sciences. Through our 147 national organisations, academic institutional members and individual members, we represent over four million pharmacists and pharmaceutical scientists around the world. Congress Theme: Pharmacy united in the recovery of health care At this critical time, when the challenges presented […]
The 4th of November a Community of Expertise will be held for which you have been invited. The presenters will be Annet Rozema, Mirjam Keulen & Marcel Hoefnagel from CBG, The Netherlands, UNICOM WP 2. Substances have been the topic of the UNICOM Community of Expertise before and this is not a surprise as substances […]
Organized by ISfTeH A one-of-a-kind meeting to discuss successful business models, opportunities in emerging markets, the challenges, and solutions for cybersecurity and international regulatory navigation.* The International Society for Telemedicine and eHealth (ISfTeH) is a federation of 45 national professional associations in the Telemedicine and eHealth space globally. The society also has institutional, corporate, and […]
The 2022 edition of pHealth will emphasize the interrelated aspects of pHealth, i.e. advanced digital health ecosystems. In that context, mobile technologies, micro-nano-bio smart systems, bio-data management and analytics, machine learning, artificial intelligence and robotics for personalized health, the Health Internet of Things (HIoT), systems medicine, public health and virtual care. UNICOM WP1 intends to […]
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 […]
Georg NEUWIRTHER will present UNICOM on May 5th at 10.00 AM. GERMAN SOCIETY FOR REGULATORY AFFAIRS (DGRA) The German Society for Regulatory Affairs e.V. is a scientific specialist society in the field of drug approval. It sees itself as a communication platform for employees in the approval departments of the pharmaceutical industry, authorities and scientific […]
Central thema: Administrable products : Based on relationship between manufactured and administrable dose form, - NoMA's solution to meet needs in clinical practice. REGISTER
Public webinar intended for business, developers and technical audiences working for industry and national competent authorities that are interested in learning more about the Product Management Service (PMS) development progress and related activities. PMS aims to deliver comprehensive and consolidated human medicinal product data (Centrally Authorised Products (CAPs) and Non-CAPs) from different sources. The webinar will be an occasion […]
This webinar is targeted at all European NCAs, eHealth competence centers and Industry (EMR, MPDs, HCP and Patient facing Apps). It will present and discuss the approach porposed by IHE to test and validate IDMP data (using UNICOM resources). The result of this webinar will feed the content of the IHE hacktathon which will take […]
UNICOM partner will orchestrate a cross border use case in the interoperability showcase. GNOMON will also make one cross border presentation in the tech leaders stage in the exhibition hall.
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Unicom developments around IDMP from a NCA (AGES) perspective by George Neuwirther IDMP Ontology by Heiner Oberkampf and Raphael Sergent EU-SRS by Annet Rozema
A report on progress and challenges from the Global IDMP Working Group (GIDWG), about substances. The presentation will give an overview of the GIDWG work on global alignment of substances, the role of a global substance ID in the medicinal product lifecycle and the challenges faced. The presentation will also demonstrate how a new resource […]
In the context of the IHE-Europe Connectathon WEEK 2023 | Connectathon in Rennes France and in parrallel to the French eHealth week. Looking across the landscape of IDMP implementation, the UNICOM project aims to develop the following testing scenarios as part of the UNICOM Test Lab: • Submission of variations When a pharmaceutical company needs […]
REGISTER NOW FOR THIS EVENT Advanced FHIR training: How to track changes on a medicinal product? UNICOM is happy to invite all of you to the 4th NCA FHIR training on October 13 10-12 CEST. This webinar focus topic is: “How to track changes on a medicinal product?” "Provenance" in the Variation FHIR message: Free text […]
Agenda: Introduction to Fimea Medicinal product database demo Lessons learned Priority actions expected from EMA Speakers: Joonas Tuominen (Fimea) Anu Ollikainen (Fimea) Markus Mäkelä (Fimea) Juha Jokimäki (Solita Finland Oy)
Unicom will be presenting all the results of WP2 related to SUBSTANCES
Annet ROSEMA from CBG in the Netherlands, Christian HAYE from GS1 and Frit Stulp will represent UNICOM during this event where UNICOM will be the red string of most strategic sessions. Have a look at the agenda: https://informaconnect.com/global-pharmaceutical-regulatory-affairs/agenda/1/
Across the UNICOM project we have been actively developing a number of standards-based resources, including FHIR Implementation Guides, a Product Lifecycle Management portal (with EMA), an IDMP database, a substitution service for cross-border dispensation, and a few patient facing apps with dedicated API’s to access medicinal product information (with Gravitate Health). These resources are meant […]
For National Competent Authorities, IDMP implementation is not an option and is already legally compulsory for pharmacovigilance. Industry has already started to submit data in the IDMP format for CAP products variation forms and this will soon be extended to all other forms. NCAs need thus to : Adapt their IT systems (and all other […]
UNICOM Day - ensure that any medicine and what it contains can be accurately identified anywhere in the world. Improve patient safety and enable better healthcare for all Agenda: 9:30 AM - 9:35 AM: Welcome and Introduction (Alexander Berler - GNOMON) SESSION 1 9:35 - 10:00 AM: The promise of IDMP interoperability: the challenge of […]
The webinar is opened to all the staff of all Medicinal Products Agencies. If you want to be invited, send a mail to 1 Welcome: Georg, Sonja Noel 2: PHAROS - Implementation of ISO-IDMP Concepts: Georg, Sonja 3: PHAROS - Importing eAF data based on the new FHIR format (Variation of CPs): Sonja, Noel, […]
This year’s ePI Summit was hosted by ROTE LISTE®. In an era where innovation is transforming every industry, the pharmaceutical sector is no exception. This year’s summit has explored the latest developments, opportunities, and challenges in electronic product information. UNICOM explained why it - together with EMA- can provide a solid foundation to the topic. See: […]
The UNICOM project has been working to improve patient safety and enable better healthcare for all, through the implementation of IDMP related standards and terminologies within a variety of processes and systems across the landscape of medicinal product development, use and evaluation. Our key focus has been on the provision of safe medication data, using […]
Breakthrough 2024 is the must-attend event for life sciences leaders across the globe. It’s the one place where leaders like you engage in the brightest, forward-looking life sciences industry conversations and hear the latest LifeSphere announcements. Bringing together industry experts, pharmaceutical leaders, and regulatory authorities, Breakthrough 2024 will explore the transformation of intelligent automation - […]
UNICOM is hosting a workshop that aims to engage stakeholders in discussions about the advantages, challenges, obstacles, and timelines related to the implementation and utilization of IDMP in the clinical realm. This exclusive, one-day event, accessible by invitation only, is designed to showcase the advancements achieved within the UNICOM project and underscore the ongoing efforts […]
UNICOM presentation by Robert VDS for a conglomerate of universities, tech and business schools, eager to build innovative implementations. Link to presentation: https://unicom-project.eu/wp-content/uploads/2024/04/unicomGroningenApril2024.pdf
This event is not only about presenting the major results achieved by UNICOM over the last four years. It will first of all aim at anchoring those results in a long term perspective and make sure IDMP is part of any major implementation project related to the identification of medicinal products. SEE THE AGENDA: https://unicom-project.eu/wp-content/uploads/2024/02/UNICOM_FinalConference_Agenda_Invitation.pdf […]
Venue: Onsite: COCIR Office, Brussels Online, link will be sent after Registration Description: Multiple interoperability-focused technical artefacts have been developed during the UNICOM project. These artefacts describe how conformant digital health solutions will participate in standards adherent data exchanges. Several European Ecosystems as EHTEL or COCIR members that provide solutions that target European and/or International […]
UNICOM will be represented by NOMA, the Norwegian Medicinal Products Agency, during the Radical Health Festivalin Helsinki in a session dedicated to Interoperability - Beyond Techonology, Towards People and Systems Talking to Each Other If data is the lifeblood of an information-driven health system, interoperability is the cornerstone for implementing prevention and precision at scale. […]
The SNOMED CT in Europe conference will be held from May 22-23, 2024 at the Pullman Brussels Centre Midi hotel in Belgium. This inaugural event will feature speakers and stakeholders from across Europe. If you are involved in clinical terminology policy and implementation in Europe then this is the event for you. In addition to hearing presentations from influential […]
The webinar will be organised by UNICOM partner HARVARD MEDICAL SCHOOL and has as key objective to update the American interested audience about UNICOM results and discuss in particular some elements of divergence of major importance between the EU and the US . 🗓️ Wed, 05/22/2024 - 12:00 - 13:30 EST (18:00-19:30 CEST) Register Now! […]
The UNICOM Innovation Action has received funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement No. 875299.
