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Up-scaling the global univocal identification of medicines


Assessment framework socio-economic impact
Estonia: Progress report on implementation

M14 M26 M38 M54

Croatia: Progress report on implementation

M14 M26 M38 M54

Procedures for use of IDMP in Personalised Medicine
Guidelines to implement IDMP in National eHealth Services
Guidelines for cross-border semantic interoperability, V1; V2

M18 M54

Guidelines for Cross-Border ePrescription / eDispensation V1; V2

M12, M48

Interim report on cost-benefit data collection

Interim report on costbenefit data collection

Endorsed Implementation Plan for Substance Management
Report on link between IDMP and Pharmacotherapeutic Groups
Annual Report on Dissemination

M12 M24 M36 M54

Spain: Progress report on implementation

M14 M26 M38 M54

Technical specifications to cross-border services

Technical specifications to crossborder services

Report on education and certification programs
Best-practice ISO IDMP workshops according to needs of the NCAs

M18 M36 M48

Business Requirements Specifications for IDMP adoption in eHealth Services, V1

M6, M48

Gap and requirements analysis for CESP Dataset Module providing the IDMP compliant application dataset
Norway: Progress report on implementation

M14 M24 M38 M54

Guidance document on how MPDs should map to substance data
Ireland: Progress report on implementation

M14 M26 M38 M54

Finland: Progress report on implementation

M14 M26 M38 M54

Portugal: Progress report on implementation

M14 M26 M38 M54

IDMP Implementation guidance for pharmacy system suppliers (focus on patient medication list)

IDMP Implementation guidance for pharmacy system suppliers focus on patient medication list

Gap-Analysis report on CTS

GapAnalysis report on CTS

Gap analysis about existing and new standards and profiles
IDMP Coding Principles and Guidance for ICSRs
ISO IDMP Handbook
Sweden: Progress report on implementatio

M14 M26 M38 M54

Germany: Progress report on implementation

M14 M26 M38 M54

Implementation guidance for IDMP in MPD
Review report of the GDPR and other legal requirements
Liaison with EC, MSs and stakeholders annual report

M12 M24 M36 M54

Requirements for a new ISO logical model [platform independent]
An analysis of the IDMP MPID provided compared to that needed in MPD for clinical care and for secondary uses
Proof of Concept demonstrator report
Guidance of GDPR compliance incl. templates model contract term

M18 M40

Common minimum data set that needs to be implemented in the national NCA and eHealth solution
Semantic Specifications, V1; V2

M21 M54

Protocol and Statistical Analysis Plan for Proof of Concept Studies
Austria: Progress report on implementation

M14 M26 M38 M54

Belgium: Progress report on implementation

M14 M26 M38 M54

Dissemination approach & communication strategy


Alignment of two standard terminologies for dosage form: RxNorm fromthe National Library of Medicine for the United States and EDQM from theEuropean Directorate for the Quality in Medicines and Healthcarefor Europe

Author(s): Natalie Karapetian, Robert Vander Stichele, Yuri Quintana
Published in: Scientific article published in International Journal of Medical Informatics 104826, Issue Volume 165, September 2022,, 2022, ISSN 1386-5056
Publisher: Elsevier BV
DOI: 10.1016/j.ijmedinf.2022.104826

How Granular Can a Dose Form Be Described? Considering EDQM Standard Terms for a Global Terminology

Author(s): Robert H. Vander Stichele; Joseph Roumier; Dirk van Nimwegen
Published in: Applied Sciences; Volume 12; Issue 9; Pages: 4337, Issue 2, 2022, ISSN 2078-2489
Publisher: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/app12094337

How to ensure we can track and trace global use of COVID-19 vaccines?

Author(s): Robert H. Vander Stichele, Christian Hay, Malin Fladvad, Miriam C.J.M. Sturkenboom, Robert T. Chen
Published in: Vaccine, Issue 39/2, 2021, Page(s) 176-179, ISSN 0264-410X
Publisher: Elsevier BV
DOI: 10.1016/j.vaccine.2020.11.055

Medicinal Product Data Standardisation – Prerequisite for Efficient Data ExchangeBetween Stakeholders and Impact on the (Inter)National Health Systems Medicinal Product Data Standardisation in the Agency for Medicinal Products and Medical Devices(HALMED)

Author(s): Sanja Grčić Plečko, Maja Fatiga, Dubravka Sudić
Published in: eTELEMED 2022 : The Fourteenth International Conference on eHealth, Telemedicine, and Social Medicine, 2022, ISBN 978-1-61208-984-3
Publisher: international Journal on Advances in Life Sciences

Will The Implementation of ISO/CEN Standards for Global Identification of Medicinal Products (IDMP) Make Any Difference for Pharmaco-Epidemiology?

Author(s): Robert H. Vander Stichele, MD – University of Ghent Med School, University of Ghent, Belgium, Gent, Oost-Vlaanderen, Belgium Co-Author(s) Miriam C. Sturkenboom, PharmD, PhD, FISPE – prof. dr., University Medical Center Utrecht, Utrecht, Utrecht, Netherlands Carlos Duran – Julius Center for Health Sciences and Primary Care, Department of Data Science & Biostatistics, University Medical Cent
Published in: Proceeding of the 2022 ICTH conference in Oslo, Issue 1123, 2022
Publisher: ICPE

Identification of Medicinal Products: Providing an Educational Framework

Author(s): Hans Gille, Robert Stegwee
Published in: Proceeding of the pHealth conference Identification of Medicinal Products, Issue Volume 299: pHealth 2022, 2022, Page(s) 271 - 274
Publisher: IOS Press
DOI: 10.3233/shti220997

Ensuring COVID-19 Vaccine Traceability

Author(s): Author: Prof. Dr Robert Vander Stichele | Senior Research Consultant | European Institute of Innovation through Health Data (I-HD), Ghent University | Ghent | Belgium Author: Christian Hay | Sr Consultant Healthcare | GS1 Global Office | ISO TC 215, WG 6 | Brussels | Belgium Author: Malin Fladvad | Product Portfolio Manager | WHO Uppsala Monitoring Centre | Uppsala | Sweden Author: Dr Robert T. Ch
Published in: healthmanagement, Issue volume 21, 2021, ISSN 1377-7629
Publisher: HealthManagement

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