
MoH
11 Projects, page 1 of 3
Open Access Mandate for Publications assignment_turned_in Project2015 - 2019Partners:UT, MOU, INSERM, NTNU, BIOMEDICAL RESEARCH FOUNDATION, ACADEMY OF ATHENS +21 partnersUT,MOU,INSERM,NTNU,BIOMEDICAL RESEARCH FOUNDATION, ACADEMY OF ATHENS,BCR,KLINIKUM RECHTS DER ISAR DER TECHNISCHEN UNIVERSITAT MUNCHEN,LBMC,IARC,SNSF,Academy of Athens,BBMRI-ERIC,IOR,Lukasiewicz - PORT,Uppsala University,LUMC,Charité - University Medicine Berlin,MoH,GERMAN CANCER RESEARCH CENTER,IRCCS,WHO,KI,SWISS BIOBANKING PLATFORM,FAU,UCL,DEÜFunder: European Commission Project Code: 676550Overall Budget: 4,949,450 EURFunder Contribution: 4,949,450 EURBBMRI-ERIC: the Biobanking and BioMolecular resources Research Infrastructure - European Research Infrastructure Consortium, aims to establish, operate and develop a Pan-European distributed research infrastructure in order to facilitate the access to biological resources as well as facilities and to support high quality biomolecular and biomedical research. The ADOPT BBMRI-ERIC proposal aims at boosting and accelerating implementation of BBMRI-ERIC and its services. Its main deliverables are designed to complete or launch the construction of key Common Services of the Research Infrastructure as required for ESFRI-projects "under implementation", reflecting the targets of the European Research Area (ERA). One of the challenges in the post-genomic era is the research on common complex diseases, such as cancer, diabetes and Alzheimer’s disease. Revealing these diseases will depend critically on the study of human biological samples and data from large numbers of patients and healthy individuals. The EU’s ageing population is will result in an increase in many of those diseases and consequently an increased healthcare expenditure for senior citizens. BBMRI-ERIC is a specific European asset having become a fundamental component in addressing the ongoing and future requirements particularly of Europe's health service frameworks, including competitiveness and innovativeness of health-related industries. Its implementation is essential for the understanding of the diversity of human diseases, biological samples and corresponding data, which are required for the development of any new drug or diagnostic assay and are, therefore, critical for the advancement in health research, ultimately leading to personalised medicine. BBMRI-ERIC will provide a gateway access to the collections of the European research community, expertise and services building on the outcome of ADOPT BBMRI-ERIC.
more_vert Open Access Mandate for Publications and Research data assignment_turned_in Project2022 - 2029Partners:NIPH, LNS, INSERM, UCD, Public Health +42 partnersNIPH,LNS,INSERM,UCD,Public Health,LSMU,MU,RIVM,UBA,Sciensano (Belgium),NIJZ,BfR,DEPA,ISS,EU,HEALTH BOARD HB,DECC,ISCIII,NVSPL,Aristotle University of Thessaloniki,Ministry of Health,RSU,Ministry of Health,CIPH,ANSES,VITO,BMEL,MoH,FIOH,NNGYK,University of Iceland,IPH MNE,DCU,FML,IRIS CR INSTITUTE OF HEALTH INFORMATION AND STATISTICS OF THE CZECH REPUBLIC,JSI,CSO-MOH,BPI,THL,INSA,CSIC,SEPA,NIOM,Environment Agency Austria,EPA,EEA,SMUFunder: European Commission Project Code: 101057014Overall Budget: 400,000,000 EURFunder Contribution: 200,000,000 EURPARC is an EU-wide research and innovation partnership programme to support EU and national chemical risk assessment and risk management bodies with new data, knowledge, methods, networks and skills to address current, emerging and novel chemical safety challenges. PARC will facilitate the transition to next generation risk assessment to better protect human health and the environment, in line with the Green Deal?s zero-pollution ambition for a toxic free environment and will be an enabler for the future EU ?Chemicals Strategy for Sustainability?. It builds in part on the work undertaken and experience acquired in past and on-going research and innovation actions, but goes beyond by its vocation to establish an EU-wide risk assessment hub of excellence. To contribute to several expected impacts of destination 2 ?Living and working in a health-promoting environment?, PARC will organise the activities to reach three specific objectives: - An EU-wide sustainable cross-disciplinary network to identify and agree on research and innovation needs and to support research uptake into regulatory chemical risk assessment. - Joint EU research and innovation activities responding to identified priorities in support of current regulatory risk assessment processes for chemical substances and to emerging challenges. - Strengthening existing capacities and building new transdisciplinary platforms to support chemical risk assessment. The Partnership brings together Ministries and national public health and risk assessment agencies, as well as research organisations and academia from almost all of EU Member States. Representatives of Directorates-General of the EC and EU agencies involved in the monitoring of chemicals and the assessment of risks are also participating. PARC will meet the needs of risk assessment agencies to better anticipate emerging risks and respond to the challenges and priorities of the new European policies.
more_vert Open Access Mandate for Publications assignment_turned_in Project2017 - 2018Partners:FZJ, CyI, SG, MoH, Ministry of Agriculture, Natural Resources and Environment +2 partnersFZJ,CyI,SG,MoH,Ministry of Agriculture, Natural Resources and Environment,HYPERION SYSTEMS ENGINEERING LTD,Ministry of Transport, Communications and WorksFunder: European Commission Project Code: 763558Overall Budget: 396,750 EURFunder Contribution: 396,750 EURThe project will upgrade the Computation-based Science and Technology Research Center of The Cyprus Institute (CyI) into a Centre of Excellence in Simulation and Data Science (SIMDAS) in Cyprus by teaming it with the Forschungszentrum Jülich (FZJ). Local partners are three public institutions as holders and providers of key data, the Departments of Antiquities, and Meteorology, and the Nicosia General Hospital, and two SMEs, Hyperion Systems Engineering, and SignalGeneriX connecting the center directly to commercial applications. During Phase-1 a comprehensive business plan for the six-year development of the center will be prepared with a detailed research, innovation and educational roadmap, governance structure, outreach and sustainability plan. Outreach and dissemination activities will engage the research communities, governmental institutions, and industry. The long-term vision of the SIMDAS project to be realized in Phase-2 revolves around five themes: i) Simulation and data science fundamentals, tools and services: Develop methodologies, tools and services, including mathematical modeling, scalable data analytics and simulations algorithms, statistics, data management, mining, security and visualization, under a Transversal Lab. ii) Simulation and data-driven research: Enable scientific breakthroughs in the key areas of Digital Cultural Heritage, Health and Life Sciences, Solar Energy, Earth System Science and Physical Sciences. iii) Government and Industry: Pursue applications of tangible innovation potential in partnership with public and private institutions utilizing the industry expertise and structures of FZJ. iv) Education: Expand graduate educational and training programs in SIMDAS. v) Infrastructure: Design and build the knowledge environment and infrastructure for a sustainable operation and provisioning of computing and data-intensive services to the broader user communities, and promote the science hub role of CyI in the Eastern Mediterranean.
more_vert Open Access Mandate for Publications assignment_turned_in Project2009 - 2012Partners:AIDFM, KI, INSERM, Federale Overheidsdienst Volksgezondheid, Veiligheid van de Voedselketen en Leefmilieu, Public Health +32 partnersAIDFM,KI,INSERM,Federale Overheidsdienst Volksgezondheid, Veiligheid van de Voedselketen en Leefmilieu,Public Health,FDHA,THL,National Institute for Health Development,IMI,UBA,NIPH,HEALTH PROTECTION AGENCY HPA,NIOM,BIPRO GMBH,Health Service Executive,DGUV,EHSI,SZU,ISS,Centrul de Mediu si Sanatate,HEAL,NHRF,Environment Agency Austria,Cefic,RIVM,LIST,ISCIII,JRC,Ministry of Health,OKI,UCPH,Úrad verejného zdravotníctva SR,VITO,JSI,MoH,KUL,Vytautas Magnus University (VMU)Funder: European Commission Project Code: 244237more_vert Open Access Mandate for Publications and Research data assignment_turned_in Project2016 - 2019Partners:CAU, SWISSTOM AG, PANAXEA, LINNEUNIVERSITETET, MoH +7 partnersCAU,SWISSTOM AG,PANAXEA,LINNEUNIVERSITETET,MoH,Amsterdam UMC,MUHEC,UNIGE,UCL,SENTEC AG,BIOMEDICAL RESEARCH FOUNDATION IBE/BRF,STUDIO FIFIELD SRLFunder: European Commission Project Code: 668259Overall Budget: 5,537,140 EURFunder Contribution: 4,234,330 EUREach year 15 million babies are born prematurely and many suffer from respiratory failure due to immaturity of the lung and lack of control of breathing. Although respiratory support, especially mechanical ventilation, can improve their survival, it also causes severe injury to the vulnerable lung resulting in severe and chronic pulmonary morbidity lasting in to adulthood. Heterogeneity of lung aeration, resulting in areas of lung over inflation and lung collapse, plays a crucial part in the risk of mortality and morbidity due to respiratory failure. This distribution of lung aeration cannot be detected by currently available bedside monitoring tools and imaging methods. Thus, an imaging technique for continuous non-invasive bedside monitoring of infants lung function is urgently needed. In order to address this, CRADL will use EIT technology to establish a monitoring tool for interventions in the paediatric population. Electrical impedance tomography (EIT) is a non-radiative, inexpensive technique that can facilitate real time dynamic monitoring of lung aeration, and recent studies have shown that it is effective in monitoring aeration in preterm babies. CRADL will show how EIT can provide new cost effective, easy to use, respiratory management tools and clinical protocols that can be universally adopted to reduce deaths and disability in preterm babies by delivering a tool that provides continuous, non-invasive, radiation free, bedside information on regional lung aeration and ventilation during daily clinical care of (preterm) infants and children with respiratory failure. CRADL will also assess the effectiveness, efficacy and safety of such a system in guiding respiratory management and supportive care of the most common causes of paediatric respiratory failure (respiratory distress syndrome, bronchiolitis and acute respiratory distress syndrome), with the final goal of reducing short and long term adverse effects of disease and its treatment in this populat
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