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BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20240522T180000
DTEND;TZID=Europe/Berlin:20240522T193000
DTSTAMP:20260501T113605
CREATED:20240502T124045Z
LAST-MODIFIED:20240507T093711Z
UID:10025-1716400800-1716406200@unicom-project.eu
SUMMARY:Sharing UNICOM results with the US audience
DESCRIPTION: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 . \n \n \n\n🗓️ Wed\, 05/22/2024 – 12:00 – 13:30 EST (18:00-19:30 CEST)\nRegister Now!\n\nMore info\nDive into the International Organization for Standardization (ISO) Identification of Medicinal Products (IDMP) standards\, a pivotal initiative reshaping global pharmacovigilance and healthcare interoperability. \nWe’ll explore the necessity of harmonizing clinical practices\, integrating medical device and pharma data management\, and the strategic importance of a unified European health data space. \nDr. Robert Stegwee will discuss IDMP’s integration with UNICOM and collaboration among stakeholders\, drawing from his expertise in health IT and healthcare interoperability standards. \nDr. Robert Vander Stichele\, a clinical pharmacologist\, will explore the clinical and pharmacovigilance use cases of IDMP. \nDr. Ron Fitzmartin from the FDA will share regulatory perspectives\, emphasizing the importance of standardized data in regulatory reviews. \nModerated by Dr. Yuri Quintana\, a leader in developing digital health systems for enhanced clinical care. \nWho Should Attend?\nRegulatory agencies\, healthcare providers\, the pharmaceutical industry\, and anyone interested in transforming healthcare standards and practices. \nKey Takeaways:\n1. Deep understanding of IDMP implementation challenges & advancements globally\n2. Varied implications for regulatory bodies\, providers & pharma industry\nActionable steps: Adopt IDMP in national systems\, enhance data sharing\, participate in collaborative IDMP testing & improvement \nABOUT UNICOM\nThe UNICOM project is financed by the European Commission within the framework of the Research and Innovation Program “Horizon 2020”\, this action has a budget of 21 million euros\, with an EC funding of 19 million euros. The consortium is composed of 70 organizations\, including 18 European countries and the United States\, who are either beneficiaries or observers. UNICOM will focus on the development of the IDMP set of standards (Identification of medicinal and pharmaceutical products) of the International Organization for Standardization (ISO)\, its testing\, implementation\, and dissemination for regulatory purposes by the National Pharmaceutical Agencies for global pharmacovigilance and for the advancement of European cross-border dispensing. Learn more at https://unicom-project.eu \nABOUT DCI NETWORK\nThe DCI Network brings together top thought leaders and decision-makers from the private sector\, government\, non-profits\, and academia to discuss emerging opportunities in digital health\, accelerate innovation and generate value from health data. The Network will create a consortium to develop roadmaps for aggregating large amounts of healthcare data from disparate stakeholders to accelerate the discussion of high-impact biomedical discoveries leading to healthcare delivery improvement. Learn more at https://www.dcinetwork.org
URL:https://unicom-project.eu/event/sharing-unicom-results-with-the-us-audience/
LOCATION:Virtual
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20240514T100000
DTEND;TZID=Europe/Berlin:20240514T150000
DTSTAMP:20260501T113605
CREATED:20240430T152914Z
LAST-MODIFIED:20240430T152914Z
UID:10022-1715680800-1715698800@unicom-project.eu
SUMMARY:UNICOM handover to Industry
DESCRIPTION:Venue: \n\nOnsite: COCIR Office\, Brussels\nOnline\, link will be sent after\nRegistration\n\n\nDescription: \nMultiple 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 digital health markets will wish to be aware of these specifications\, inform the development of the final implementation guidance\, and (potentially) be certified as conformant so that they may participate in RFPs that mandate the specs. This workshop aims to start the sharing process between UNICOM’s artefacts and the industry ecosystem. \nAs a starting point\, IHE who is a collaborative of vendors\, digital health users and key experts from health informatics standards organizations such as HL7\, DICOM\, SNOMED and others will leverage UNICOM artefacts as a “running start” by the IHE Pharmacy Technical Committee (TC) and HL7 Europe Technical Coordination Team. With vendor and user input\, the content will be finalized\, balloted\, and published as a set of global digital health specifications by IHE International. European (UNICOM) contextual requirements will be published as an HL7 FHIR IG (EU realm) and IHE Volume-4 addendum to the global specs; this addendum is governed by IHE Europe and aligned with work developed under the HL7 Europe EU realm. The work will be further supported and developed under XpanDH project and supported by the European EHRxF Standards and Policy Hub in formation by the xShare project. COCIR members and other industry players are invited to market-shape by participating in the development of the specifications and their related normative requirements and/or by conformance-testing their products at IHE test events. \n  \nKey Objectives of the Workshop: \n– Present UNICOM technical artefacts and their implications for the industry. \n– Discuss the handover of UNICOM artefacts to global technical artifact organizations. \n  \nProgram: \n\n\n\nTime\nTopic\n\n\n10:00 – 12:30\n  \nPresentations part : \n\nPresentation of the UNICOM artefacts and how they can benefit industry\nPresentation of the different groups that will collect the artefact and reuse them (IHE Pharmacy\, HL7 Europe\, etc…)\nPresentation of the conformance steps\n\n\n\n\n12:30 – 13:30\n  \nLunch Break\n\n\n13:30 – 15:30\n  \nInteractive part\, ask the participants: \n\nHow can your organization contribute and leverage these artefacts? What will be the impact?\nWhat are the benefits of certifying digital health solutions as conformant to these specifications?\nWhat additional information or support would be beneficial for your organization to fully leverage UNICOM artefacts?\nHow can the industry collectively ensure the successful adoption and implementation of these specifications?\n\n\n\n\n\n 
URL:https://unicom-project.eu/event/unicom-handover-to-industry/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20240425T080000
DTEND;TZID=Europe/Berlin:20240426T170000
DTSTAMP:20260501T113605
CREATED:20240103T112232Z
LAST-MODIFIED:20240422T135215Z
UID:9748-1714032000-1714150800@unicom-project.eu
SUMMARY:UNICOM FINAL EVENT
DESCRIPTION: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. \nSEE THE AGENDA: https://unicom-project.eu/wp-content/uploads/2024/02/UNICOM_FinalConference_Agenda_Invitation.pdf \nREGISTER: https://www.tickettailor.com/events/ehtel/1166419
URL:https://unicom-project.eu/event/unicom-final-event/
LOCATION:Brussels\, Belgium
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/png:https://unicom-project.eu/wp-content/uploads/2024/01/UNICOM-FINAL-EVENT.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20240322
DTEND;VALUE=DATE:20240323
DTSTAMP:20260501T113605
CREATED:20240209T184827Z
LAST-MODIFIED:20240209T184827Z
UID:9806-1711065600-1711151999@unicom-project.eu
SUMMARY:IDMP in the clinical world workshop (under invitation only)
DESCRIPTION: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\ndesigned to showcase the advancements achieved within the UNICOM project and underscore the ongoing efforts to unlock the benefits of IDMP.\nThis workshop serves as a crucial occasion to involve participants who were not all actively part of the project discussions. The event’s preparation will leverage the final key papers and deliverables produced by various representatives across the value chain within UNICOM. \n  \nInvited stakeholders include:\n– National Competent Authorities\n– eHealth national organisations\n– Medicinal Product Dictionaries providers\n– EHR vendors\n– Pharmacovigilance specialists\n– SDO representatives\n– Hospital Pharmacists\n– University representatives
URL:https://unicom-project.eu/event/idmp-in-the-clinical-world-workshop-under-invitation-only/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20240308T150000
DTEND;TZID=Europe/Berlin:20240308T163000
DTSTAMP:20260501T113605
CREATED:20240209T175226Z
LAST-MODIFIED:20240213T180228Z
UID:9800-1709910000-1709915400@unicom-project.eu
SUMMARY:UNICOM Community of Expertise: Standards for Safe Medication Data
DESCRIPTION: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 standards. This Community of Expertise looks back on what we have accomplished\, both within UNICOM and in our relations with other projects\, and how standards are evolving for use by the key actors that will deliver on our promise for improved patient safety: the patients and the healthcare professionals\, supported by timely information and knowledge from pharmaceutical experts. \nOur main objective for this Community of Expertise is to explore the ways in which our collaborative efforts on standards for safe medication data can be taken forward in the immediate and longer-term future\, to enable better healthcare for all. \nEverybody is welcome but REGISTRATION is compulsory. \nPresenters: \nChristian Hay – UNICOM WP1\, ISO/TC 215 Health Informatics WG6 Pharmacy and Medicines Business\, GS1 \nRobert Stegwee – UNICOM WP1\, CEN/TC 251 Health Informatics \n  \nPanellists: \nTo be announced \n  \nModerators: \nEsther Peelen\, UNICOM WP1\, Nictiz \nZain Ishfaq\, UNICOM WP1\, Nictiz
URL:https://unicom-project.eu/event/unicom-community-of-expertise-standards-for-safe-medication-data/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20240228T140000
DTEND;TZID=Europe/Berlin:20240228T153000
DTSTAMP:20260501T113605
CREATED:20240209T184423Z
LAST-MODIFIED:20240221T091122Z
UID:9804-1709128800-1709134200@unicom-project.eu
SUMMARY:Knowledge Transfer Webinar: AGES (Austria) in focus
DESCRIPTION:The webinar is opened to all the staff of all Medicinal Products Agencies. \nIf you want to be invited\, send a mail to unicom@ehtel.eu \n1 Welcome:  Georg\, Sonja Noel \n2: PHAROS – Implementation of ISO-IDMP Concepts: Georg\, Sonja \n3: PHAROS – Importing eAF data based on the new FHIR format (Variation of CPs): Sonja\, Noel\, Georg \n4: Integration of EMA SPOR services  – OMS data: tbc \n5: Integration of EMA SPOR services  – RMS data: Noel \n6: Integration of EMA SPOR services  – SMS data: Noel \n7: Providing Medicinal Product Data  in FHIR 5.0 format – Outlook: Noel \n8: Conclusions \n 
URL:https://unicom-project.eu/event/knowledge-transfer-webinar-ages-austria-in-focus/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20240118T093000
DTEND;TZID=Europe/Berlin:20240118T150000
DTSTAMP:20260501T113605
CREATED:20240111T161221Z
LAST-MODIFIED:20240111T161945Z
UID:9774-1705570200-1705590000@unicom-project.eu
SUMMARY:IDMP Medicinal products Substitution Workshop: UNICOM day in ATHENS
DESCRIPTION:UNICOM Day – ensure that any medicine and what it contains can be accurately identified anywhere in the world. \nImprove patient safety and enable better healthcare for all \nAgenda: \n\n9:30 AM – 9:35 AM: Welcome and Introduction (Alexander Berler – GNOMON)\n\nSESSION 1 \n\n9:35 – 10:00 AM: The promise of IDMP interoperability: the challenge of safe product identification\, how IDMP can bridge that gap and the need to implement it in different standards\, regions\, and use cases (Rutt Lindström – TEHIK\, José Costa Teixeira – IHE)\n\n\n10:00 AM – 10:20 AM: IDMP in Greek context – the national view (Kostas Mathioudakis – IDIKA)\n10:20 AM – 10:35 AM: IDMP in the context of Pharma Innovation – (Ioannis Kotsiopoulos – Pharma Innovation Forum)\n\n\n10:35 AM – 11:00 AM: IDMP in crossborder context (Alberto Zanini – ARIA\, Rutt Lindström – TEHIK)\n11:00 AM – 11:30 AM: Coffee Break\n\n  \nSESSION 2 \n\n11:30 AM – 11:55 PM: \n\nTopic: the IHE Methodology and its application to UNICOM Test Lab use cases;  \nPresenter: Derek Ritz and José Costa Teixeira – IHE \n\n11:55 AM – 12:10 PM: \n\nIDMP Specifications and Tools (Use Cases\, UNICOM IG\, UNICOM transactions\, UNICOM Toolbox etc?) – Including data onboarding \nPresenter: José Costa Teixeira – IHE \n\n12:10 PM – 13:30 PM: IDMP medication substitution workshop\n\n12:10 – 12:25 Substitution & PFA’s Demonstration (Nicole Veggioti – DataWizard\, Argiris Gkogkidis – GNOMON\, Haralampos Karanikas – GNOMON\, Dimitris Kounalakis – GNOMON)\n12:25 – 13:30 Discussion/workshop on transaction related to product selection: searching and comparing products to find equivalents and potential substitutes\, based on IDMP data on FHIR.\n13:30 lunch break end of workshop
URL:https://unicom-project.eu/event/idmp-medicinal-products-substitution-workshop-unicom-day-in-athens/
LOCATION:Athens\, ROYAL OLYMPIC\, Greece
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/png:https://unicom-project.eu/wp-content/uploads/2024/01/athens.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20231206T130000
DTEND;TZID=Europe/Berlin:20231206T143000
DTSTAMP:20260501T113605
CREATED:20231024T094911Z
LAST-MODIFIED:20231024T100538Z
UID:9507-1701867600-1701873000@unicom-project.eu
SUMMARY:Knowledge Transfer Webinar: Germany (BFarm) in focus
DESCRIPTION:
URL:https://unicom-project.eu/event/knowledge-transfer-webinar-germany-bfarm-in-focus/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20231128
DTEND;VALUE=DATE:20231201
DTSTAMP:20260501T113605
CREATED:20230505T082232Z
LAST-MODIFIED:20230920T161332Z
UID:9289-1701129600-1701388799@unicom-project.eu
SUMMARY:7th Consortium meeting: Open to all European NCAs - Ghent - Belgium
DESCRIPTION: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. \nNCAs need thus to : \n\nAdapt their IT systems (and all other systems which consume their data) to make them IDMP compliant as soon as possible.\nConvert their own legacy data to IDMP\nAnalyse which IDMP compliant data need to be made available to end-users systems and how they can be delivered.\n\nDuring this event\, we intend to cover the following (non-exhaustive) questions: \n\nWhat could be seen as the ideal reference workplan? Which steps need to be followed?\nHow and when to involve business in the process?\nWhat does it cost to become IDMP compliant?\nWhat are the possible implementation scenarios?\nWhat are the risks and how can they be mitigated?\nWhat is missing today? Who will provide it and when?\nWhat level of expertise related to IDMP and FHIR need to be developed internally and what can be externalised?\nWhat kind of new competencies do you need to have/develop in your agency?\nWhat needs to be done in order to be able to distribute the data? And how best to integrate other types of data (such as reimbursement data)?\nWhat kind of support should we expect from EMA and what should be made available in priority?\n\nThe IDMP journey requires a lot of (new) competencies\, and we believe that a representation of both IT and Business would be very much beneficial. \nThe information collected prior and during the meeting will also help the project to formulate important recommendations to key actors such as the European Commission\, EMA\, the Global IDMP Working Group and the Standards Development organisations. It will also provide the rationale for a new project proposal which could be discussed with the EU Commission. \nWhere will the event take place? \nThe event will conveniently take place in the historic city of Ghent\, Belgium which is less than one hour by train from the main Belgian airport. \nThe UNICOM partners will meet on November 28TH but NCAs which are not members of the consortium are invited  to join us on the 29th . All participants are also warmly invited to attend the UNICOM partners EHTEL and  I~HD conferences on November 29- Dec 1 where topics of strategic importance for NCAs such as the use of real-world evidence or patient safety will be the central focus. Several strategic initiatives and projects will be present to exchange their experience with the I~HD and UNICOM communities. \nHere is a short decsrition of the global event: \nThe Digital Health and Data Week is a three-day event\, the result of the collaboration between EHTEL\, I~HD\, and the UNICOM project consortium. They are partnering to work on digital health solutions and data that result in the provision of real value for care and research.  All three days of the week include complementary topics\, and their content builds on each other. \nToday\, it has never been so important for all digital health stakeholders to network and learn from each other’s experiences. \nIn order to make it worth your time and effort to come in person to Ghent\, i~HD\, EHTEL\, and UNICOM\, are partnering together to create a unique Digital Health and Data Week. All three organisations are collaborating in organising a combined set of events during the last week of November 2023\, in Ghent (Belgium). \n\nOn 28 November 2023\, UNICOM is arranging its seventh consortium meeting\nOn 29 November 2023\, EHTEL organises its 2023 Thought Leader Symposium\nOn 30 November and 1 December 2023\, i~HD holds its annual conference\, the Health Data Forum.\n\nAll three days of the week include complementary topics\, and their content builds on each other. \n  \n 
URL:https://unicom-project.eu/event/4th-consortium-meeting-open-to-all-european-ncas-ghent-belgium/
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/jpeg:https://unicom-project.eu/wp-content/uploads/2023/05/DSC_1342b-scaled.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20231103T150000
DTEND;TZID=Europe/Berlin:20231103T163000
DTSTAMP:20260501T113605
CREATED:20230928T160101Z
LAST-MODIFIED:20231018T084735Z
UID:9449-1699023600-1699029000@unicom-project.eu
SUMMARY:UNICOM Community of Expertise: Putting UNICOM ressources to the test
DESCRIPTION: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). \nThese resources are meant to live on after the end of the UNICOM project and to be used by a wealth of stakeholders across the UNICOM landscape. To facilitate the use of these resources\, we have identified a limited set of use cases for which we intend to set up testing facilities\, using the IHE Methodology for conformance testing. By doing that\, we enable stakeholders to engage in rigorous testing of the interaction of their products and services with these UNICOM resources. \nDuring the UNICOM Day on 28 September\, during the IHE Europe Connectathon\, we shared\, discussed and detailed our work thus far. \nThis webinar builds on the diszcussions which took place in Rennes and is  meant to provide insight into the possibilities to be offered to our stakeholders\, to identify next steps for the selected use cases and surface future needs for new use cases. \nThe webinar is an excellent opportunity for new people and organisations to engage in the development of use cases and testing scenarios that will put the UNICOM resources to the test and make them a valuable asset beyond the life of the UNICOM project. \nSpeakers: \n· Sofia Franconi (WP1\, IHE Europe) \n· Alexander Berler (WP6\, IHE Europe) \n· Derek Ritz (IHE International) \nPanelists: \n· Raphael Sergent (WP1\, ISO/TC 215) and Robert Stegwee (WP1\, CEN/TC 251):  eAF use case \n· Zain Ishfaq and Esther Peelen (both WP1\, Nictiz): NCA to MPD use case \n· Robert Vander Stichele (WP1\, WP8\, i~HD): NCA to NCPeH use case \n· Angela Ferrara (WP7\, Aria)  cross-border dispensation use case \n· Argiris Gkoghidis (WP6\, Gnomon) and Nicole Veggiotti (WP8\, Datawizard): Patient facing apps use case \nREGISTER HERE\n 
URL:https://unicom-project.eu/event/unicom-community-of-expertise-connecting-unicom-to-the-ihe-community/
LOCATION:Virtual
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/jpeg:https://unicom-project.eu/wp-content/uploads/2020/02/ihe-3.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20231023
DTEND;VALUE=DATE:20231026
DTSTAMP:20260501T113605
CREATED:20230324T175057Z
LAST-MODIFIED:20230324T175057Z
UID:9218-1698019200-1698278399@unicom-project.eu
SUMMARY:Global Pharmaceutical Regulatory Affairs Summit
DESCRIPTION:Unicom will be presenting all the results of WP2 related to SUBSTANCES
URL:https://unicom-project.eu/event/global-pharmaceutical-regulatory-affairs-summit/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20231020T140000
DTEND;TZID=Europe/Berlin:20231020T153000
DTSTAMP:20260501T113605
CREATED:20230809T154359Z
LAST-MODIFIED:20231012T120801Z
UID:9397-1697810400-1697815800@unicom-project.eu
SUMMARY:Knowledge Transfer Webinar: FINLAND in focus
DESCRIPTION:Agenda: \n\nIntroduction to Fimea\nMedicinal product database demo\nLessons learned\nPriority actions expected from EMA\n\nSpeakers: \nJoonas Tuominen (Fimea) \nAnu Ollikainen (Fimea) \nMarkus Mäkelä (Fimea) \nJuha Jokimäki (Solita Finland Oy)
URL:https://unicom-project.eu/event/knowledge-transfer-webinar-finland-in-focus-2/
LOCATION:Online Event – URL on Registration
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/jpeg:https://unicom-project.eu/wp-content/uploads/2020/02/fimea-1.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20231013T100000
DTEND;TZID=Europe/Berlin:20231013T120000
DTSTAMP:20260501T113605
CREATED:20230126T103807Z
LAST-MODIFIED:20230531T095700Z
UID:9196-1697191200-1697198400@unicom-project.eu
SUMMARY:Advanced FHIR training: How to import application form data into IT systems
DESCRIPTION:REGISTER NOW FOR THIS EVENT \n\n\n\n\nAdvanced FHIR training: How to track changes on a medicinal product?\nUNICOM is happy to invite all of you to the 4th NCA FHIR training on October 13 10-12 CEST.\n\nThis webinar focus topic is: “How to track changes on a medicinal product?”\n“Provenance” in the Variation FHIR message: \n\nFree text changes\nOrganisation changes\nMedicinal Product changes (IDMP fields)\n\nFor your personal convenience\, we provide you here below with the links to the videos of the three previous FHIR related trainings. \n►Get an overview of the full product:FHIR Training: The Medicinal Product part of FHIR\n–> (recording) <– \n►Get an overview of the variation message: FHIR Training: FHIR on Variations\n–> (recording) <– \n  \n►Top 10 most wanted IDMP fields: FHIR Training: Top 10 IDMP fields through XPath\n–> (recording) <– \n\nFri\, Oct 13\, 10:00 AM – 12:00 PM (CEST)\n 
URL:https://unicom-project.eu/event/advanced-fhir-training-how-to-import-application-form-data-into-it-systems/
LOCATION:Online Event – URL on Registration
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/png:https://unicom-project.eu/wp-content/uploads/2021/05/fihr-connecthaton.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20230928
DTEND;VALUE=DATE:20230929
DTSTAMP:20260501T113605
CREATED:20230407T142518Z
LAST-MODIFIED:20230921T090228Z
UID:9249-1695859200-1695945599@unicom-project.eu
SUMMARY:UNICOM day IHE Connectathon in Rennes
DESCRIPTION:In the context of the IHE-Europe Connectathon WEEK 2023 | Connectathon in Rennes France and in parrallel to the French eHealth week. \nLooking across the landscape of IDMP implementation\, the UNICOM project aims to develop the following testing scenarios as part of the UNICOM Test Lab:\n• Submission of variations\nWhen a pharmaceutical company needs to apply for market authorization for a variation of an already authorized medicinal product\, how can a FHIR/IDMP-compliant exchange of information with the appropriate national competent authority (NCA) support such an application?\n• Updates to the MPD\nWhen changes to the national list of authorized medicinal products are published by the local NCA\, how can a FHIR/IDMP-compliant exchange of information facilitate the updates in the local Medicinal Product Dictionaries (MPDs)? And how are they made available to the variety of clinical systems using the MPD data?\n• Updates to the NCPeH product database\nWhen changes to the national list of authorized medicinal products are published by the local NCA\, how can a FHIR/IDMP-compliant exchange of information facilitate the updates in the product database for cross-border ePrescribing and Dispensing\, as needed by the National Contact Point for eHealth (NCPeH)\n• Including substitution in eDispensation\nHow does the local pharmacy apply substitution rules\, based on the CDA/IDMP-compliant data in a cross-border ePrescription\, and communicate the actual dispensed medication back in the CDA/IDMPcompliant dispensation record?\n• Product lookup for patient facing apps\nHow can a patient use a FHIR/IDMP-compliant multilanguage representation of over-the-counter (OTC) medication to safely substitute their common medication by the locally available brand\, checking for intolerances and interactions? \nEach team will present the highlights of their work during the in-person UNICOM Day on September 28\, 2023 in Rennes\, France. The objective is to further develop the testing strategy in conjunction with IHE Europe\, to make sure that conformance with IDMP related standards and terminologies can be systematically tested in the future\, even when the UNICOM project has finished. \nHere is the agenda of the day: \n \nWe encourage you to register without delay  for the UNICOM Day in Rennes\, France on SEPTEMBER 28 through THIS LINK 
URL:https://unicom-project.eu/event/unicom-ihe-hachathon/
LOCATION:Rennes\, France
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/jpeg:https://unicom-project.eu/wp-content/uploads/2020/02/ihe-3.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230915T150000
DTEND;TZID=Europe/Berlin:20230915T163000
DTSTAMP:20260501T113605
CREATED:20230904T080033Z
LAST-MODIFIED:20230912T121642Z
UID:9409-1694790000-1694795400@unicom-project.eu
SUMMARY:UNICOM Community of Expertise: Global alignment on substances based on the ISO IDMP and the SRS software
DESCRIPTION:A  report on progress and challenges from the Global IDMP Working Group (GIDWG)\, about substances. \nThe 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. \nThe presentation will also demonstrate how a new resource for substances could be requested using a FHIR Task in an asynchronous process that may or may not involve human interaction and demonstrate how the resource for substances will look\, and can be used as references from other resources such as EU-SRS. \n  \nPresenters: \nOlof Lagerlund\, Magnus Wallberg (WHO-UMC) \nMagnus Wallberg [WHO-UMC} \nAnnet Rozema (or colleague) (EU-SRS team at CBG/MEB) \n  \nPanellist: \nRobert Vander Stichele (i~HD) \nMonica Harry (SNOMED International) \nNorman Schmuff (FDA) \nModerators: \nChristian Hay\, UNICOM WP1\, ISO/TC 215 WG6 Pharmacy and Medicines Business\, GS1 \nRobert Stegwee\, UNICOM WP1\, CEN TC 251 \n  \nRegistration: CLICK HERE
URL:https://unicom-project.eu/event/unicom-community-of-expertise-global-alignment-on-substances-based-on-the-iso-idmp-and-the-srs-software/
LOCATION:Virtual
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/jpeg:https://unicom-project.eu/wp-content/uploads/2023/01/EU-SRS-Logo-full.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230626T140000
DTEND;TZID=Europe/Berlin:20230626T153000
DTSTAMP:20260501T113605
CREATED:20230330T160412Z
LAST-MODIFIED:20230331T111336Z
UID:9235-1687788000-1687793400@unicom-project.eu
SUMMARY:Knowledge transfer webinar: SPAIN in Focus
DESCRIPTION:You may already REGISTER
URL:https://unicom-project.eu/event/knowledge-transfer-webinar-spain-in-focus/
LOCATION:Virtual
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/png:https://unicom-project.eu/wp-content/uploads/2023/03/aemps.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230530T143000
DTEND;TZID=Europe/Berlin:20230530T160000
DTSTAMP:20260501T113605
CREATED:20230407T142207Z
LAST-MODIFIED:20230531T094601Z
UID:9242-1685457000-1685462400@unicom-project.eu
SUMMARY:Putting resources developed by UNICOM to the test: Preparing the UNICOM IHE Connecthathon
DESCRIPTION: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 pkace in Rennes (France) on September 28th. \nIHE-Europe Connectathon WEEK 2023 | Connectathon. \nWATCH THE WEBINAR\nMore info: \nUNICOM Work Packages 6 and 1 are pleased to announce an upcoming webinar 30 May 14:30-16:00 CET. This webinar will prelude the UNICOM Day\, taking place 28 September 2023\, during the IHE Europe Connectathon week in Rennes\, France.  \n Join us to find out how the IHE structured and globally proven way of testing will help you to get your systems seamlessly communicating with the ones of your partners. Together with you we will define the testing scenario’s that will actually facilitate interoperability and conformance testing with IDMP.  \n  \nTest Lab \nThe 30 May webinar will set off the UNICOM Test Lab calendar and the Test Lab scenario’s. With guidance of WP6 and WP1 you will be creating the testing scenario’s that will be piloted the next months. UNICOM Software factory in WP6 has developed several components that will get you started!  \nTogether we will present and discuss the results of the test lab experience during the UNICOM Day September 28. \n Are you working at an NCA\, the Pharma Industry\, a Medicinal Product Dictionary Provider\, an eHealth agency\, an EHR vendor or a Patient app provider and involved in IDMP implementation? Then this webinar is for you! \n Of course there will be plenty of opportunity to address your questions. We encourage all those interested in testing their implementation of IDMP-identifiers and attributes to attend this webinar on the 30th of May at 14h30.” \nFootnote: the two-day event ‘IHE-Europe Experience Days’ will take place 26 and 27 September. You might want to take the opportunity to get updated on all relevant European and Global developments in interoperability in Healthcare! Just have a look at the programme and registration details here.
URL:https://unicom-project.eu/event/putting-resources-developed-by-unicom-to-the-test-preparing-the-unicom-ihe-hechtaton/
LOCATION:Rennes\, France
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230530T100000
DTEND;TZID=Europe/Berlin:20230530T113000
DTSTAMP:20260501T113605
CREATED:20230508T093917Z
LAST-MODIFIED:20230508T095017Z
UID:9294-1685440800-1685446200@unicom-project.eu
SUMMARY:EMA Product Management Service (PMS) progress webinar
DESCRIPTION: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. \nPMS aims to deliver comprehensive and consolidated human medicinal product data (Centrally Authorised Products (CAPs) and Non-CAPs) from different sources. \nThe webinar will be an occasion for the audience to meet the PMS product owners\, ask questions and learn more about the deliverables achieved to support web-based electronic Application Forms (eAFs) as well as the planned PMS activities driving the implementation of ISO standards for the identification of medicinal products (IDMP) in the EU/EEA.
URL:https://unicom-project.eu/event/ema-product-management-service-pms-progress-webinar/
LOCATION:Virtual
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/png:https://unicom-project.eu/wp-content/uploads/2021/02/logo-ema.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230524T120000
DTEND;TZID=Europe/Berlin:20230524T133000
DTSTAMP:20260501T113605
CREATED:20230330T155955Z
LAST-MODIFIED:20230330T172720Z
UID:9233-1684929600-1684935000@unicom-project.eu
SUMMARY:Knowledge transfer Webinar: Norway (NOMA) in focus
DESCRIPTION:Central thema: Administrable products :  Based on relationship between manufactured and administrable dose form\, – NoMA’s solution to meet needs in clinical practice. \nREGISTER
URL:https://unicom-project.eu/event/knowledge-transfer-webinar-norway-noma-in-focus/
LOCATION:Virtual
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/jpeg:https://unicom-project.eu/wp-content/uploads/2020/03/NoMA_logo-scaled.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230421T150000
DTEND;TZID=Europe/Berlin:20230421T163000
DTSTAMP:20260501T113605
CREATED:20230324T180216Z
LAST-MODIFIED:20230324T180326Z
UID:9220-1682089200-1682094600@unicom-project.eu
SUMMARY:Community of Expertise: IDMP data : from source to final use
DESCRIPTION:Description:\nReferring 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. \nThis Community of Expertise (CoE) will provide opportunity :\nfor industry to present their perspective and needs\, with large international companies\, with SME facing IT investments to implement IDMP\, and with advisers supporting IDMP implementation in companies and organisations;\nfor Medicinal Product Dictionaries suppliers\, with their the hub function between pharmaceutical companies\, National Competent Authorities\, on one hand\, and for their customers in the clinical space on the other hand;\nand for the consumption of these data with Pharmacovigilance. \nPresenters:\nQuentin Darrasse\, Roche Pharma\nAndreas Franken\, BAH\nStefan Peev\, NNIT\nFrederic Doc\, Vidal\nBoukje Raemaekers\, WHO-UMC \nPanellist:\nMalin Fladvad\, WHO-UMC \nModerators:\nChristian Hay\, UNICOM WP1\, ISO/TC 215 WG6 Pharmacy and Medicines Business\, GS1\nRobert Stegwee\, UNICOM WP1\, CEN TC 251 \nRegister here
URL:https://unicom-project.eu/event/community-of-expertise-idmp-data-from-source-to-final-use/
LOCATION:Webinar via Zoom
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/jpeg:https://unicom-project.eu/wp-content/uploads/2022/07/picture-WP1-e1657728267149.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20230417
DTEND;VALUE=DATE:20230421
DTSTAMP:20260501T113605
CREATED:20230329T134208Z
LAST-MODIFIED:20230329T134208Z
UID:9227-1681689600-1682035199@unicom-project.eu
SUMMARY:EMA WEBINAR WEEK
DESCRIPTION:►You can register for the relevant Webinar by selecting the link below: \n\nSPOR and XEVMPD Data Governance – 17 April\, 10:00-12:00 CET – https://ema-europa.webex.com/weblink/register/r9ca0c1044ed05282d0fe236251c99a9c\nService Desk for SPOR and XEVMPD – 17 April\, 14:00-16:00 CET – https://ema-europa.webex.com/weblink/register/r1552802c0646096c101b5e62b25dfa5d\nReferentials Management Service (RMS) – 18 April\, 10:00-12:00 CET – https://ema-europa.webex.com/weblink/register/r46516995ff51d5f4383d95f05cac8e38\nOrganisation Management Service (OMS) – 18 April\, 14:00-16:00 – https://ema-europa.webex.com/weblink/register/r834ea26426a57529292e0dcffc96cb5a\nSubstance Management Service (SMS) – 19 April\, 10:00-12:00 CET – https://ema-europa.webex.com/weblink/register/ra85e8fd6945484df2ff2df4f3117a19e\nProduct Management Service (XEVMPD) – 19 April\, 14:00-16:00 CET – https://ema-europa.webex.com/weblink/register/r84045da9fedf6fdec5fd69c8d24a2c3a\nSubstance\, product\, organisation and referential (SPOR) application programming interface (API) – SPOR API – 20 April\, 10:00-12:00 CET – https://ema-europa.webex.com/weblink/register/r00e936a4aeb9d8e1ed61fac53c879858\nEMA Account Management – 20 April\, 14:00-16:00 CET – https://ema-europa.webex.com/weblink/register/r393a359debcd8d2cd14a974465c369e8
URL:https://unicom-project.eu/event/ema-webinar-week/
LOCATION:Virtual
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230413T143000
DTEND;TZID=Europe/Berlin:20230413T160000
DTSTAMP:20260501T113605
CREATED:20230324T181527Z
LAST-MODIFIED:20230330T160529Z
UID:9223-1681396200-1681401600@unicom-project.eu
SUMMARY:NCA KNOWLEDGE TRANSFER: BELGIUM IN FOCUS
DESCRIPTION:Agenda : \n\n25’ Results of the FAMHP IDMP gap analysis:\n\n1. EMA : deviations (more\, less\, different) versus ISO IDMP documents (of 2012 and 2017\, whichever is more recent)\n2. FAMHP MPM/DTS : differences with the EMA data model\n3. FAMHP approach to narrow the gaps\n\n\n10’ QUESTIONS\n15’ SAM / ePrescription : dataflow from BE NCA (and other datasources) to mandatory BE ePrescription (on SAM)\n10’ QUESTIONS\n what are the gaps in your NCA datamodel + what is your (intended) approach towards narrowing them ?
URL:https://unicom-project.eu/event/nca-knowledge-transfer-belgium-in-focus/
LOCATION:Virtual
CATEGORIES:External events related to UNICOM
ATTACH;FMTTYPE=image/jpeg:https://unicom-project.eu/wp-content/uploads/2020/02/famhp-1.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230329T133000
DTEND;TZID=Europe/Berlin:20230329T150000
DTSTAMP:20260501T113605
CREATED:20230126T103239Z
LAST-MODIFIED:20230324T181638Z
UID:9194-1680096600-1680102000@unicom-project.eu
SUMMARY:NCA Knowledge Transfer Webinar: Croatia implementation progress
DESCRIPTION:REGISTER NOW FOR THIS EVENT
URL:https://unicom-project.eu/event/nca-knowledge-transfer-webinar-croatia-implementation-progress-and-demo/
LOCATION:Online Event – URL on Registration
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230310T100000
DTEND;TZID=Europe/Berlin:20230310T120000
DTSTAMP:20260501T113605
CREATED:20230126T101626Z
LAST-MODIFIED:20230126T101626Z
UID:9192-1678442400-1678449600@unicom-project.eu
SUMMARY:Basic Training IDMP & FHIR for NCAs staff
DESCRIPTION:UNICOM is happy to announce a new series of IDMP implementation related training and knowledge transfer webinars in 2023. \nConsidering 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 implementation and that more people are informed and trained about this with the NCAs. \nFeel thus free to transfer this invitation to any person in your Agency who could possibly be impacted. \nYou need to REGISTER to have access to the webinar
URL:https://unicom-project.eu/event/basic-training-idmp-fhir-for-ncas-staff/
LOCATION:Online Event – URL on Registration
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20230124
DTEND;VALUE=DATE:20230125
DTSTAMP:20260501T113605
CREATED:20230105T111637Z
LAST-MODIFIED:20230105T111654Z
UID:9151-1674518400-1674604799@unicom-project.eu
SUMMARY:Celebration day: Transfer of substance dataset to EMA and go-live of EU-SRS
DESCRIPTION: 
URL:https://unicom-project.eu/event/celebration-day-transfer-of-substance-dataset-to-ema-and-go-live-of-eu-srs/
LOCATION:AMSTERDAM
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20230110T130000
DTEND;TZID=Europe/Berlin:20230110T140000
DTSTAMP:20260501T113605
CREATED:20230110T104906Z
LAST-MODIFIED:20230110T104906Z
UID:9156-1673355600-1673359200@unicom-project.eu
SUMMARY:5th HL7 FHIR ePI Vulcan accelerator
DESCRIPTION: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\n-> All the detailed information about the track can be found here: https://lnkd.in/eD8x3TQu \nThis is the 5th  event in the series of companion events to Vulcan ePI Project HL7 FHIR Connectathon tracks that will take place in Nevada on 14-15 January\, 2023. \nThe vision of the Gravitate Health ePI /Vulcan accelerator ePI/ eLabeling project is to define a common structure for medicinal product information that improves the patient experience and supports interoperability across the international healthcare clinical and regulatory environment.
URL:https://unicom-project.eu/event/5th-hl7-fhir-epi-vulcan-accelerator/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20221104T150000
DTEND;TZID=Europe/Berlin:20221104T163000
DTSTAMP:20260501T113605
CREATED:20221024T141028Z
LAST-MODIFIED:20221024T141028Z
UID:9051-1667574000-1667579400@unicom-project.eu
SUMMARY:UNICOM Community of Expertise: SUBSTANCE and EU-SRS
DESCRIPTION:The 4th of November a Community of Expertise will be held for which you have been invited. \nThe presenters will be Annet Rozema\, Mirjam Keulen & Marcel Hoefnagel from CBG\, The Netherlands\, UNICOM WP 2. \nSubstances have been the topic of the UNICOM Community of Expertise before and this is not a surprise as substances form one of the three pillars of medicinal product identification. Much progress has been achieved in the last twelve months \nUNICOM WP2 is tasked with setting up the EU Substance Registration System EU-SRS. \nThe EU-SRS team would like to share with you how the different substance types which are handled in EU-SRS; which fields are captured\, and howthe records are  structured. Therefore\, we provide a deep dive into the working of EU-SRS\, with a focus on explaining how Chemicals\, Polymers\, Proteins and Vaccines are handled in EU-SRS. We will show real examples of European substances records and explain some of the key choices made in how to build these records in EU-SRS. This will provide good insight in the capabilities of EU-SRS for use by the European regulatory network\, after go-live of the system. \n  \nModeration will be done by:  \nChristian Hay (UNICOM WP 1\, ISO/TC 215 WG6) \nRobert Stegwee (UNICOM WP 1\, CEN/TC 251) \n  \nRegistering for the event can be done by following the link: \nhttps://us02web.zoom.us/webinar/register/WN_FrC98CkUS_ynxEhx2BFgew \n 
URL:https://unicom-project.eu/event/unicom-community-of-expertise-substance-and-eu-srs/
LOCATION:Webinar via Zoom
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20220826T150000
DTEND;TZID=Europe/Berlin:20220826T163000
DTSTAMP:20260501T113605
CREATED:20220510T101657Z
LAST-MODIFIED:20220621T085516Z
UID:8852-1661526000-1661531400@unicom-project.eu
SUMMARY:Community of Expertise: Navigating global and national identifiers using IDMP and FHIR
DESCRIPTION:The next UNICOM Community of Expertise is scheduled on Friday 26 August 2022: \nIn 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 she knows which medication is effective in her home country. In addition to finding an equivalent medicinal product available locally (the UNICOM demonstrator case) she also wants to access the pertinent electronic product information (ePI) in her own language (the Gravitate Health case). This requires careful and safe navigation across the respective national identifiers of the medicinal products involved\, using the global linkage between them. This session highlights the choices and discussions taking place on the FHIR resources to be used and the services to be developed for these purposes. \nPresenters:             Esther Peelen (UNICOM WP 1\, Nictiz)\n                        Craig Anderson (Gravitate Health\, Vulcan\, Pfizer)\n                        Leonora Grandia (UNICOM WPs 8 and 9\, Z-Index)\n                        Giorgio Cangioli (UNICOM WP 1\, HL7 Europe) \nPanelists:             Jens Villadsen (Gravitate Health\, HL7 Europe\, Trifork)\n                        Hugh Glover (UNICOM FHIR IDMP Server\, Vulcan\, Blue Wave Informatics)\n                        Rik Smithies (EMA FHIR Consultant\, Vulcan\, NProgram)\n                        José Costa Teixeira (UNICOM WPs 1 and 6\, IHE Pharmacy) \nModerators:      Christian Hay (UNICOM WP 1\, ISO/TC 215 WG6)\n                  Robert Stegwee (UNICOM WP 1\, CEN/TC 251) \nYou can register with the following link: https://us02web.zoom.us/webinar/register/WN_eIcAxPw4QmOYEwbugv5ObA
URL:https://unicom-project.eu/event/community-of-expertise-unicom-demonstrator-idmp-to-support-patient-empowerment/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20220621T110000
DTEND;TZID=Europe/Berlin:20220621T110000
DTSTAMP:20260501T113605
CREATED:20220531T125658Z
LAST-MODIFIED:20220531T130637Z
UID:8869-1655809200-1655809200@unicom-project.eu
SUMMARY:National Competent Centers knowledge exchange webinar: Focus on Ireland
DESCRIPTION:Those webinars are meant to facilitate an early and detailed cross-fertlisation between European National Competent Authorities. \nIreland (HPRA) will be presnting its current sttaus on its road toward IDMP implementation. \nAll staff of all European agencies are warmly welcome to attend. \nIf you have not received an invitation but would like to attend\, please send a mail to unicom@ehtel.eu \nif you are not part of a NCA but have specific interest in participating\, explain it shortly in a mail to unicom@ehtel.eu
URL:https://unicom-project.eu/event/national-competent-centers-knowledge-exchange-webinar-focus-on-ireland/
CATEGORIES:External events related to UNICOM
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=Europe/Berlin:20220516T100000
DTEND;TZID=Europe/Berlin:20220516T120000
DTSTAMP:20260501T113605
CREATED:20220510T101227Z
LAST-MODIFIED:20220510T101746Z
UID:8850-1652695200-1652702400@unicom-project.eu
SUMMARY:DADI-PMS Webinar: Variations Form for Human Medicinal Products - What will happen at Go-Live
DESCRIPTION:REGISTER
URL:https://unicom-project.eu/event/dadi-pms-webinar-variations-form-for-human-medicinal-products-what-will-happen-at-go-live/
CATEGORIES:External events related to UNICOM
END:VEVENT
END:VCALENDAR