28th HL7 FHIR Connectathon -virtual 13-15 September 2021

Virtual

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 […]

First UNICOM transatlantic meeting

Virtual

​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 […]

HL7 Europe Webinar: Interoperable proof of vacination – Implementation approaches across Europe

Virtual

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, […]

Recurring

WP5/6/7 – Workshop on the eHealth services and their connections/dependencies

Virtual

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 […]

Recurring

WP5/6/7 – Workshop on the eHealth services and their connections/dependencies

Virtual

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 […]

20th Regulatory Affairs and Pharmacovigilance webinar

Virtual

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 […]