Up-scaling the global univocal identification of medicines

CORDIS oferuje możliwość skorzystania z odnośników do publicznie dostępnych publikacji i rezultatów projektów realizowanych w ramach programów ramowych HORYZONT.

Odnośniki do rezultatów i publikacji związanych z poszczególnymi projektami 7PR, a także odnośniki do niektórych konkretnych kategorii wyników, takich jak zbiory danych i oprogramowanie, są dynamicznie pobierane z systemu OpenAIRE .

Rezultaty

UNICOM Smart Substitution component
Develop demonstrators, including videos
UNICOM User Portal Reference implementation for eP/eD and PS
UNICOM IDMP DB API
UNICOM Semantic components

Delivery of selected ISO IDMP medicinal product data for crossborder pilots

Assessment framework socio-economic impact
Procedures for use of IDMP in Personalised Medicine
Guidelines to implement IDMP in National eHealth Services
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
Technical specifications to cross-border services

Technical specifications to crossborder services

Report on education and certification programs
Gap and requirements analysis for CESP Dataset Module providing the IDMP compliant application dataset
Guidance document on how MPDs should map to substance data
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
Implementation guidance for IDMP in MPD
Review report of the GDPR and other legal requirements
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
Protocol and Statistical Analysis Plan for Proof of Concept Studies
Dissemination approach & communication strategy

Publikacje

Frameworks, Dimensions, Definitions of Aspects, and Assessment Methods for the Appraisal of Quality of Health Data for Secondary Use: Comprehensive Overview of Reviews

Autorzy: Jens Declerck, Dipak Kalra, Robert Vander Stichele, Pascal Coorevits
Opublikowane w: JMIR Medical Informatics, Numer 12, 2024, Strona(/y) e51560, ISSN 2291-9694
Wydawca: JMIR Med
DOI: 10.2196/51560

Identification of Drugs Acting as Perpetrators in Common Drug Interactions in a Cohort of Geriatric Patients from Southern Italy and Analysis of the Gene Polymorphisms That Affect Their Interacting Potential

Autorzy: Mauro Cataldi, Camilla Celentano, Leonardo Bencivenga, Michele Arcopinto, Chiara Resnati, Annalaura Manes, Loreta Dodani, Lucia Comnes, Robert Vander Stichele, Dipak Kalra, Giuseppe Rengo, Francesco Giallauria, Ugo Trama, Nicola Ferrara, Antonio Cittadini, Maurizio Taglialatela
Opublikowane w: Geriatrics, Numer 8, 2023, Strona(/y) 84, ISSN 2308-3417
Wydawca: MDPI AG
DOI: 10.3390/geriatrics8050084

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

Autorzy: Natalie Karapetian, Robert Vander Stichele, Yuri Quintana
Opublikowane w: Scientific article published in International Journal of Medical Informatics 104826, Numer Volume 165, September 2022,, 2022, ISSN 1386-5056
Wydawca: 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

Autorzy: Robert H. Vander Stichele; Joseph Roumier; Dirk van Nimwegen
Opublikowane w: Applied Sciences; Volume 12; Numer 9; Pages: 4337, Numer 2, 2022, ISSN 2078-2489
Wydawca: Multidisciplinary Digital Publishing Institute (MDPI)
DOI: 10.3390/app12094337

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

Autorzy: Robert H. Vander Stichele, Christian Hay, Malin Fladvad, Miriam C.J.M. Sturkenboom, Robert T. Chen
Opublikowane w: Vaccine, Numer 39/2, 2021, Strona(/y) 176-179, ISSN 0264-410X
Wydawca: 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)

Autorzy: Sanja Grčić Plečko, Maja Fatiga, Dubravka Sudić
Opublikowane w: eTELEMED 2022 : The Fourteenth International Conference on eHealth, Telemedicine, and Social Medicine, 2022, ISBN 978-1-61208-984-3
Wydawca: 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?

Autorzy: 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
Opublikowane w: Proceeding of the 2022 ICTH conference in Oslo, Numer 1123, 2022
Wydawca: ICPE

Identification of Medicinal Products: Providing an Educational Framework

Autorzy: Hans Gille, Robert Stegwee
Opublikowane w: Proceeding of the pHealth conference Identification of Medicinal Products, Numer Volume 299: pHealth 2022, 2022, Strona(/y) 271 - 274
Wydawca: IOS Press
DOI: 10.3233/shti220997

Ensuring COVID-19 Vaccine Traceability

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