National Competent Authorities for Medicinal Products – Page 3

- OCTOBER 23, 2020
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Learning from each other: The UNICOM NCAs knowledge exchange workshops have been launched!
Learning from each other: The UNICOM NCAs knowledge exchange workshops have been launched! Twelve National Competent Authorities for medicinal products are actively involved in the UNICOM project. They are pioneering the implementation of the identification of medicinal products (IDMP) in the European Medicines Regulatory Network (EU MRN). Implementing IDMP standards in this business domain is challenging. Numerous topics have to be solved covering business, IT aspects, and dataRead more
- Georgi Georgiev
- News
- SEPTEMBER 25, 2020
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Community of Expertise webinar upcoming on Friday, 2 October, 15-16 CET: “UNICOM – Gap Analysis about existing and new standards and profiles”
Community of Expertise webinar upcoming on Friday, 2 October, 15-16 CET: ``UNICOM - Gap Analysis about existing and new standards and profiles`` The bimonthly "Community of Expertise" interactive sessions are organised by UNICOM work package 1 “IDMP-related standards and terminologies.” The webinars discuss current IDMP topics and further issues related to the identification of medicinalRead more
- Stephan Schug
- News
- SEPTEMBER 17, 2020
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Webinar (21 Sept, 14:00 CET): Towards European data spaces for medicines – Semantic interoperability for patient safety
UNICOM contributes to the webinar: Towards European data spaces for medicines - Semantic interoperability for patient safety, that is being organised Monday, 21 September 2020, 14:00 – 15:30 CET. The meeting belongs to the EHTEL “Imagining 2029” work programme. As a virtual meeting of the EHTEL/ELO Network it is part of its Moving Towards EuropeanRead more
- Stephan Schug
- News
- SEPTEMBER 4, 2020
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BADI Drug Regulatory Affairs e-Congress
The UNICOM Project – benefits from ISO IDMP/SPOR for health care professionals and patients, are presented by Peter Bachmann in the BADI Drug Regulatory Affairs e-Congress on 5 June 2020
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- Klaus Piesche
- Resources
- SEPTEMBER 4, 2020
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Goals, Activities, IDMP Implementation Challenges
Presentation on HL7 FHIR / Unicom Joint Meeting by Karl A. Stroetmann on 18 May 2020
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- Klaus Piesche
- Resources
- SEPTEMBER 4, 2020
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First reference documents of the EU-SRS – the European Substance Registration System are now available!
First reference documents of the EU-SRS – the European Substance Registration System are now available! Background EU-SRS A team of experts from the European medicines regulatory network (European Medicines Agency and national medicines authorities from the EU Member States), supported by experts from the US Food and Drug Administration (FDA) and US National Center forRead more
- Georgi Georgiev
- News

Archives

Learning from each other: The UNICOM NCAs knowledge exchange workshops have been launched!

Community of Expertise webinar upcoming on Friday, 2 October, 15-16 CET: “UNICOM – Gap Analysis about existing and new standards and profiles”

Webinar (21 Sept, 14:00 CET): Towards European data spaces for medicines – Semantic interoperability for patient safety

BADI Drug Regulatory Affairs e-Congress

Goals, Activities, IDMP Implementation Challenges

First reference documents of the EU-SRS – the European Substance Registration System are now available!

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