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Open Medicine: Advancing International Standards for Healthcare

Learn how the openMedicine project supports the implementation of international standards for healthcare, with a focus on IDMP, ePrescription, and Dispense Medicinal Products. Explore the role of CEN.TC.251 and their contribution to standards coordination, production, and delivery. Stay updated on the progress and expected outcomes of these initiatives.

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Open Medicine: Advancing International Standards for Healthcare

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  1. CEN TC 251:openMedicine in a win-win perspective June 2015

  2. The link from ISOto openMedicine

  3. CEN TC 251 and openMedicine • CEN TC 251 wholeheartedly supports the work ongoing in openMedicine and contribute in various WP. • Different parts of openMedicine support the uptake of the international standards that CEN TC 251 works on. • We expect openMedicine delivering important input for international standards in preparation.

  4. ISO TC 216 WG 6work programme

  5. Our work programme • IDMP implementation guides • Medicinal product dictionary systems for health care • ePrescription • Requirements for the record of Dispense Medicinal Products

  6. IDMP : Graphicaloverview 19844 20440 20451 20443

  7. IDMP summarised roadmap Dates refer to the meeting whendecisionistaken April 2015

  8. Requirements for Medicinal product dictionary systems for health care (prEN ISO DTS 19256) The MPD-system does not exist on its own.It is a component of a larger clinical and/or pharmacy information system.

  9. Requirementsforelectronicprescriptions (EN ISO DIS 17523 ) • Requirements on • Identification of the patient • Authentication of the prescription (metadata) • Identification of the prescriber • Identification of the prescribed product • Prescription information • Alignment with Guidelines on ePrescriptions dataset for electronic exchange under cross-border Directive 2011/24/EU (R1) • FDIS ballot to be opened late August 2015

  10. Requirementsfor the record of Dispense Medicinal Products(prEN ISO DTS 19293) CEN TC 215 reorganisation paper states that TC 251 plays a role in • Standards coordination • Standards production • Standards delivery

  11. Requirementsfor the record of Dispense Medicinal Products(prEN ISO DTS 19293) Here a concrete example of the interactions: • The EU openMedicine project addresses • standards coordination (ISO, HL7, GS1, etc.), • standards production (input for the development of ISO/DTS 19293 Requirements for the record of Dispensed Medicinal Products) and • standards delivery (promote IDMP).

  12. Requirementsfor the record of Dispense Medicinal Products(prEN ISO DTS 19293) • prEN ISO DTS 19293 is currently on hold • Will leverage outcomes from openMedicine • Expected to be balloted as DTS in 4th quarter 2016

  13. Contact Christian Hay Convenor ISO TC 216, WG 6 Sr Consultant Healthcare GS1 Global Office Tel +41 21 825 32 19 Mob +41 76 369 10 54 christian.hay@gs1.org

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