Examples of using Reference networks in English and their translations into Croatian
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Reference Networks to tackle rare and complex diseases.
List of pilot European Reference Networks for Rare Diseases.
Member States are encouraged to facilitate the development of the European reference networks.
Centres of expertise and European reference networks for rare diseases.
European reference networks shall have at least three of the following objectives.
These criteria and conditions shall ensure, inter alia,that European reference networks.
European reference networks will represent an ideal opportunity to introduce and test telemedicine in the EU.
Develop and publish criteria for establishing andevaluating European reference networks;(c).
European Reference Networks are virtual networks that bring together experts from across the EU.
Develop, adopt and publish the procedures for establishing andevaluating European reference networks;
It supports the development of"European Reference Networks" bringing together, on a voluntary basis, specialised centres of expertise already recognised in Europe.
Experience gained by these projects helped to design a legal framework andwill serve future European Reference Networks.
Through European reference networks patients with rare or complex diseases benefit from the best expertise from across Europe without even leaving their home country.
This Directive should therefore give incentives to Member States to reinforce the continued development of European reference networks.
Encourages further development of European Reference Networks of medical expertise, broadening cooperation between EU countries, with added benefits to health technology assessments and e-health.
Support the development of the tools facilitating cooperation andinteroperability of the European Reference Networks for rare diseases.
In March the first 24 European Reference Networks for rare and complex diseases were launched, involving more than 900 highly specialised healthcare units from over 300 hospitals in 25 EU Member States, plus Norway.
Make use of the Directive 2011/24/EU on the application of patients' rights in cross-border healthcare to bring together European Reference Networks on rare diseases.
On 1 March 2017, the first 24 European Reference Networks officially started their activities, based on the framework provided by the European Commission, driven by the involved healthcare providers and national health authorities.
Before the adoption of Directive 2011/24/EU, the Commission supported 10 specific pilot European Reference Networks for Rare Diseases through the EU Health Programme.
The Directive aims to identify already established centres of expertise andto encourage voluntary participation of healthcare providers in the future European Reference Networks.
European reference networks are based on the voluntary participation of their members, but the Commission should develop criteria and conditions that the networks should be required to fulfil in order to receive support from the Commission.
The Directive on the application of patients' rights in cross-border healthcare provides further opportunities for increased cooperation through European Reference Networks between healthcare providers and centres of expertise.
Reference networks will promote cooperation among highly specialised providers across Member States, allowing patients with low prevalence, complex or rare diseases to access high quality care.
The Recommendation focuses on i definition, codification and inventory of rare diseases, ii research,iii European reference networks, iv gathering expertise at EU level, v empowerment of patient organisations, and vi sustainability.
Interoperable eHealth systems will support the implementation of European Reference Networks envisaged by the Directive on patients' rights in cross-border care27, which will have to deploy telemedicine at a large scale to be successful in providing treatment.
Notes that in 2016 DG SANTE launched the first product of the‘State of Health in the EU' initiative, the joint OECD-Commission report‘Health at a Glance: Europe 2016',created 23 European Reference Networks on rare diseases, set up a task force on antimicrobial resistance and established a new EU platform on food losses and food waste;
Directive 2011/24/EU establishes cooperation between the Member States' health systems for addressing common challenges such as access to healthcare,in particular through the recently launched European Reference Networks; the cooperation on Health Technology Assessment; and the cooperation in the eHealth Network and within the Digital Single Market.
Science and Technology:Virtual Reference Network, first of its kind in SEE.
European Reference Network: Coordinators training, methodology and tools.