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This project is partially funded by the European Commission
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Deliverables
Del. NoDeliverable NameDelivery date
D1.1User needs and requirementsM6
D1.2Patient Safety management process , modeling and scenario based designM12, M36
D1.3REMINE legal implicationM24, M36
D1.4Impact assessmentM24, M36
D2.1First Revision of Digital Input Multimedia Data Platform (DIMDP)M18
D2.2Third Revision of Digital Input Multimedia Data Plantform (DIMDP)M32
D2.3First revision of real time RAPS alerting for patient safetyM14
D2.4Third revision of Real Time RAPS alerting for patient safetyM32
D2.5First revision of data communication securityM12
D2.6Third revision of data communication securityM32
D3.1Data&Process model System Semantic specifications and rulesM12
D3.2Classification and identification of risk event using BPM processM12, M24
D3.3First revision of Data&Model process system frameworkM12
D3.4Third revision of Data&Model process system frameworkM32
D3.5First revision of WP3 framework (including RTRMAS and PPRMAS)M15
D3.6Third revision of WP3 framework (including RTRMAS and PPRMAS),M32
D3.7First revision of the data mining and knowledge extraction moduleM18
D3.8Third revision of the data mining and knowledge extraction moduleM32
D4.1RAPS Taxonomy approach and definitionM6
D4.2RAPS domain ontologyM12, M18
D4.3RAPS application ontologyM12, M24
D4.4Multilingual RAPS taxonomyM24
D4.5Documentation of formalized guidelinesM18
D4.6Documentation of prototypal implementation of the guidelines execution engineM20, M26
D4.7First release of Adverse Risk Management Support SystemM18
D4.8Third release of Adverse Risk Management Support SystemM33
D5.1H-ERP component interface coordinator first revisionM12
D5.2H-ERP component interface coordinator third revisionM33
D5.3Wrapper engine for: LabM12, M24, M36
D5.4Wrapper engine for: DrugsM12, M24, M36
D5.5Wrapper engine for: NosocomialM12, M24, M36
D5.6Wrapper engine for: Clinical PathwayM12, M24, M36
D5.7Technical Specification Adverse Clinical rules model specialized for patent safetyM18, M24, M30
D5.8First Revision of adverse clinical rules model specialized for patient safety componentM18
D6.3First Platform REMINE prototypeM18
D6.4Third Platform REMINE prototypeM33
D7.1UDTB deployment and assessmentM12, M36
D7.3REMINE first pilot platformM18
D7.4REMINE  third Pilots PlatformM33
D8.1Project WebsiteM3
D8.2Dissemination PlanM6
D8.3Harmonization plan for the REMINE frameworkM12, M36
D8.4Promotional/informational materials and multimedia dissemination materialsM12, M24, M36
D8.5Report on the dissemination, a networking activities and dissemination activities on standardization bodiesM12, M24, M36
D8.6State of Art about the intellectual property rightsM24, M36
D8.7Skills analysis and training strategy and planM24
D8.8Accessible e-Training platformM24
D8.9Report on Training activitiesM24, M36