UNICOM presentation at 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
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 […]