presentation of the eso ehealth-interop -v7...Ò public presentation of the report under...

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L L CEN/CENELEC/ETSI CEN/CENELEC/ETSI M403 M403 eHealth Interoperability eHealth Interoperability HL7 International Affiliates and ISO Co HL7 International Affiliates and ISO Co - - ordination ordination May 4, 2008 May 4, 2008 Presented by Presented by Melvin Reynolds Melvin Reynolds on behalf of the Project Coordination Group on behalf of the Project Coordination Group

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Page 1: Presentation of the ESO eHealth-INTEROP -v7...Ò Public presentation of the report under consultation Crete § 9-10 October 2008, connected to IHIC’08 Ò Open consultation Copenhagen

èè CEN/CENELEC/ETSICEN/CENELEC/ETSIM403 M403 –– eHealth InteroperabilityeHealth Interoperability

HL7 International Affiliates and ISO CoHL7 International Affiliates and ISO Co--ordination ordination May 4, 2008May 4, 2008

Presented by Presented by Melvin ReynoldsMelvin Reynoldson behalf of the Project Coordination Group on behalf of the Project Coordination Group

Page 2: Presentation of the ESO eHealth-INTEROP -v7...Ò Public presentation of the report under consultation Crete § 9-10 October 2008, connected to IHIC’08 Ò Open consultation Copenhagen

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Mandate M/403

ÒThe three European Standards Organisations (ESOs), CEN, CENELEC and ETSI, accepted a mandate from the European Commission

ÒM/403 aims to provide a consistent set of standards to address the needs of the rapidly-evolving field of eHealth for the benefit of future healthcare provision

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Mandate M/403

ÒeHealth and in particular the electronic health record with its three priority issues:§ patient and health practitioner identifiers;§ the patient summary;§ an emergency data set.

Ò2 phases§ First year setting up a work programme§ Three years to implement the results

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Mandate M/403 Phase 1

ÒA team of appointed experts reporting to the ESOswill:§ examine the portfolios of existing standards from the

many different organizations in the sector, including international formal bodies and industry standards consortia § perform an analysis of sector needs and § provide recommendations for specific standards

developments

ÒFollowing consultation with other international partners a work programme will be produced

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Mandate M/403 Phase 1 outcome

ÒThe resulting work programme will be the main outcome of Phase 1, it will be based on an analysis of existing standards, ongoing work and requirements, and will contain a list of proposed work items for possible standards action under phase 2 of the mandate.

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Mandate M/403 Phase 1 PT

ÒThe Project Team has been installed on 28/3/2008 with the following persons:§ Mr Melvin Reynolds, editor (UK)§ Mr Charles Parisot (France)§ Mr Pantelis Angelidis (Greece)

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Co-ordination of the work 1/2

ÒA Co-ordination Group (CG) of the three ESOs§ CEN Secretariat and TC251 Chair (CG chair)§ CENELEC Secretariat and TC62 Chair § ETSI Secretariat and eHealth Chair § NEN (CG secretariat) § EU and EFTA Secretariats - observers

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Co-ordination of the work 2/2

Ò In addition the three ESOs established a collaborative mechanism in the form of a wider co-ordination group of approximately 15 EU and international standards bodies and consortia

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Wide Coordination needed … !

Based on original by: Charles Parisot

Profile Development

Base Standards DevelopmenteHealth ProjectsInteroperability Specifications

CEN

IHTSDO

IHE

Continua

IEC/ISO JTC1

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Phase 1 Timescale (dates to put in your agenda) 1/2

Ò Wider Co-ordination group in Gothenburg§ 28 May 2008, connected to MIE

Ò Meeting to discuss the pre-final draft and to make proposals for amendments

§ July 2008

Ò Consultation on the pre-final draft § July/August 2008

Ò Final phase 1 report and work programme Public consultation

§ Sept/Oct 2008

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Phase 1 Timescale (dates to put in your agenda) 2/2

Ò Public presentation of the report under consultation Crete§ 9-10 October 2008, connected to IHIC’08

Ò Open consultation Copenhagen§ 7 November 2008, connected to WoHIT

Ò Approval of the ESOs of the work programme and Submission of the phase 1 work programme to the EC/EFTA§ Dec 2008

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eHealth-INTEROP Report

ÒBackground

ÒWorking method

Ò Inventory of requirements

Ò Inventory of standards

ÒStandards adoption lifecycle

ÒWorkplan

ÒOther content

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eHealth-INTEROP Report

ÒThe project team will bear in mind:§ The wish of the Member States to keep their autonomy;§ The goal of the EC to have joint European/global

standards and to have European policy on eHealth;§ The consequences for the working methods of the ESOs;§ the need for use cases such as the 3 priorities of the EC

but also that emerge from consulting patients, clinicians and health authorities.

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Connecting communities

Based on: Kees Molenaar, Chair CEN/TC251 Health Informatics

• IHE• Continua

• Continua

• …

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Stay tuned

Ò http://www.ehealth-interop.nen.nl

ÒMs. Shirin Golyardi, NEN, [email protected]

ÒMs. Tamara Slagter, NEN, [email protected]

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Key points

Ò eHealth-INTEROP is requirements driven and collaborative: § will populate use cases with existing international

standards when possible;§ collaborate with standards fora, consortia and SDOs.

Ò eHealth-INTEROP has a tight schedule: § Phase 1 will deliver a work programme by the end of

November 2008; § consultation will be during the summer and early autumn

2008; § please pencil in 7 November 2008 in Copenhagen to

discuss final draft.

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Questions/Comments

Thank you for your attention