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Virtual

January 2021

20th Regulatory Affairs and Pharmacovigilance webinar

January 21 @ 2:00 pm - 3:30 pm
Logo of medicines for europe

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 can support the regulatory objectives in the pharmaceutical strategy and what are the concrete steps to move forward? Panel Speakers: Hilmar Hamann, Head of Information…

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February 2021

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

February 4 @ 2:00 pm - 4:30 pm
|Recurring Event (See all)

One event on February 5, 2021 at 2:00 pm

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 and pilots planned to test the adapted technical infrastructure by UNICOM. The workshop will be organised over 2 full afternoons, across 2 days. Where: Day…

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

February 5 @ 2:00 pm - 5:10 pm
|Recurring Event (See all)

One event on February 5, 2021 at 2:00 pm

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 and pilots planned to test the adapted technical infrastructure by UNICOM. The workshop will be organised over 2 full afternoons, across 2 days. Where: Day…

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

February 25 @ 4:00 pm - 6:00 pm

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, 10 min each) Line Saele Andreassen, HL7 Europe Board of Directors, HL7 Norway, Public Health Agency of Norway Giorgio Cangioli, HL7 Europe Board of Directors,…

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June 2021

First UNICOM transatlantic meeting

June 8 @ 3:00 pm - 5:00 pm

​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 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…

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WP2 to present at IRISS meeting

June 10 @ 4:00 pm - 5:00 pm
|Recurring Event (See all)

An event every month that begins at 4:00 pm on day Second of the month, happening 36 times

Monthly IRISS meeting IRISS is a non-profit dedicated to advancing Implementation of Regulatory Information and Submission Standards for life sciences globally, see https://iriss-forum.org/.

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July 2021

WP2 to present at IRISS meeting

July 8 @ 4:00 pm - 5:00 pm
|Recurring Event (See all)

An event every month that begins at 4:00 pm on day Second of the month, happening 36 times

Monthly IRISS meeting IRISS is a non-profit dedicated to advancing Implementation of Regulatory Information and Submission Standards for life sciences globally, see https://iriss-forum.org/.

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