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! […]
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 […]
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 […]
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
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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 […]
Central thema: Administrable products : Based on relationship between manufactured and administrable dose form, - NoMA's solution to meet needs in clinical practice. REGISTER
►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 […]
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 […]
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
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 […]
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 […]
