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Overview
Lobbying Costs
9,999€
Financial year: Jan 2018 - Dec 2018
Lobbyists (Full time equivalent)
6.5 Fte (12)
Lobbyists with EP accreditation
0
High-level Commission meetings
0
Lobbying Costs over the years
-
Info
The European Institute for Innovation through Health Data (i~HD)
EU Transparency Register
957449219758-32 First registered on 01 Dec 2015
Goals / Remit
The European Institute for Innovation through Health Data (i~HD) has been formed as one of the key sustainable entities arising from the Electronic Health Records for Clinical Research (EHR4CR) and SemanticHealthNet projects, in collaboration with several other European projects and initiatives supported by the European Commission.
The vision of i~HD is to become the European organization of reference for guiding and catalyzing the best, most efficient and trustworthy uses of health data and interoperability, for optimizing health and knowledge discovery.
i~HD has been established in recognition that there is a need to tackle areas of challenge in the successful scaling up of innovations that critically rely on high quality and interoperable health data, to sustain and propagate the results of health ICT research, and to specifically address obstacles to using health data that are not being addressed by other current initiatives. It has been formed after wide consultation (...)Main EU files targeted
Undertake initiatives and lead areas of research contributing to the EC’s Digital Single Market
Develop best practices in developing semantic interoperability assets
Develop and promote codes of conduct for the reuse of health data for researchAddress
Head Office
Merebaaistraat 10
Oosterzele 9860
BELGIUMEU Office
c/o Dept. Medical Informatics & Statistics, Ghent University
Universitair ziekenhuis Gent, 5K3
Gent 9000
BELGIUM -
People
Total lobbyists declared
12
Employment time Lobbyists 100% 2 75% 2 50% 4 25% 4 Lobbyists (Full time equivalent)
6.5
Lobbyists with EP accreditation
No lobbyists with EP accreditations
Complementary Information
None declared
Person in charge of EU relations
Data not provided by Register Secretariat due to GDPR
Person with legal responsibility
Data not provided by Register Secretariat due to GDPR
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Categories
Category
III - Non-governmental organisations
Subcategory
Non-governmental organisations, platforms and networks and similar
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Networking
Affiliation
None declared
Member organisations
https://www.i-hd.eu/index.cfm/about/members/
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Financial Data
Closed financial year
Jan 2018 - Dec 2018
Lobbying costs for closed financial year
9,999€
EU grant income for closed financial year
4,659 € (Source: H2020-SC1-2016-CNECT)
Other financial info
None declared
-
EU Structures
Groups (European Commission)
eHealth Stakeholder Group#E02769 #http://ec.europa.eu/transparency/regexpert/index.cfm?do=groupDetail.groupDetail&groupID=2769 #Member #C
Groups (European Parliament)
N/A
Communication activities
i~HD is being formed as one of the key sustainable entities arising from the Electronic Health Records for Clinical Research (EHR4CR) and SemanticHealthNet projects, in collaboration with several other European projects and initiatives supported by the European Commission. i~HD has been established as a European not for profit body, registered in Belgium through Royal Assent. It will itself be governed by its member stakeholders, public and private, through an elected Board and officers. It will be financed by a mixture of membership subscriptions, fees from providing services including certification and accreditation, specific project grants and other income from education, training and expert advisory roles.
Vision
To become the European organization of reference for guiding and catalyzing the best, most efficient and trustworthy uses of health data and interoperability, for optimizing health and knowledge discovery.
Mission
To enable, coordinate, and accelerate the efficient development and deployment of interoperable and seamless eHealth solutions and research strategies, towards achieving best practices and sustainable integrated person-centred health care, to optimize health and wellness in Europe, and beyond.
Objectives
1/Championing harmonised health information and standards for capturing, curating, protecting and exchanging health data in a trustworthy, legally compliant and transparent manner using best practices. This is to enable complete and interoperable health records on individuals and populations to deliver benefits to all stakeholders , supporting and guiding the best use of standards and assets for semantic interoperability and privacy protection.
2/Providing and/or fostering capabilities to enable better quality health data, and the legitimate sharing and uses of health data.
3/Facilitating, deriving and using intelligence from health data (scientific and clinical intelligence, research, knowledge discovery, service improvement and business intelligence) through advancing the uses of:
- Electronic Health Records and Personal Health Records
- Citizen sourced data
- Mobile health sources
- Social care records
- Disease, device and quality registries
- Reimbursement claims and reporting databases
- Cohort studies and Bio Banks
- Clinical trial and electronic case report forms (eCRF)
- Other potential sources of health related data
4/ Performing and commissioning quality assessments, and conducting or overseeing quality audits of:
- Health related ICT systems and applications
- Health data6
- Personnel using health data
- Relevant organisational processes
5/ Building synergy and consensus: acting as a focal point bringing stakeholders together to share experiences, agree common priorities and approaches for maximizing the benefits of good quality and interoperable health data and the trustworthy reuse of health data, working towards convergence and cross-fertilization between stakeholders.
6/Defining and supporting the adoption of best practices in information governance, including ethics, privacy protection, and codes of conduct, relating to the trustworthy use of health data including capture, processing and sharing.
7/ Defining and driving a cohesive strategy and vision for ICT supported, person-centred care, wellness and prevention, especially from data and knowledge perspectives.
8/Creating awareness and promoting the Institute and its objectives, promoting the value of high quality health data, and delivering training and education in topics relating to its objectives.
9/Ensuring sustainability of the Institute and of initiatives within the health data ecosystem, through business model innovation and value assessment, by developing assessment frameworks and tools, and by collating and disseminating the existing and future evidence of value from catalysing the development and implementation of well-coordinated interoperable eHealth strategies and programmes.Other activities
None declared
- Meetings
Meetings
None declared
- Meetings