The document discusses the Rosetta Terminology Mapping (RTM) profile, which aims to harmonize the use of existing medical device terminology standards. The profile specifies a set of tables that map proprietary device terms to standardized terms, and define correct units of measure and enumerated values. This will promote semantic interoperability between devices and healthcare IT systems. The profile also identifies gaps in current standards to facilitate further development of clinical decision support and research using medical device data.
This document provides an implementation guide for creating Personal Healthcare Monitoring Reports (PHMRs) using the Clinical Document Architecture Release 2 (CDA R2) standard. It defines constraints and requirements for the CDA header and sections. The guide is intended for use internationally. It was last updated in August 2010 as a second draft for trial use and comment. Feedback on the draft is requested.
The document describes a data model for representing clinical measurement terms and their relationships in a structured nomenclature. Key elements include base concepts, differentiating criteria sets to specialize concepts, and semantic links to define relationships between descriptive elements. The model supports building systematic names in a directed way and representing synonyms and language variations.
The document provides an overview of the Fennec UI, outlining its themes of maximizing screen space for content while minimizing typing. It then walks through the basic controls, navigation, notifications, add-ons/downloads/preferences, identity features, and desktop integration via Weave. Key aspects highlighted include finger-friendly design, quick lookup scenarios, and linking to the desktop Firefox experience.
The document discusses factors in interaction design for mobile experiences. It notes that while mobile browsing can be similar to stationary browsing, it is important to focus on how it is different. Some differences come from the mobile device itself, like small screens and direct manipulation interfaces, while other differences come from the user context of being mobile, interruptible, and having changing social and physical contexts. The document suggests designers consider the technical system, the user and their context, and the tasks users aim to complete.
Healthcare Robotics is a field that deals with combined medical & technological fields. Robots in healthcare are helping the medical personals for performing tasks that take lot of time & also making the medical process safer & more cost-effective. Healthcare Robotics is helpful for performing surgeries at small places & to handle risky substances. Healthcare Robotics finds a wide application is medical procedures, while some more technologies are under research. Use of robotics in Healthcare is increasing due to factors like; rise in number of elderly population, increase in number of minimally invasive surgical (MIS), rise in number of systems providing high resolution imaging, fine control & haptic feedback, reduction in treatment cost with increased quality, increase in technical advancement, severe shortage of medical personals, etc. Therefore, the Healthcare Robotics Market is anticipated to expand and has tremendous scope during the forecast period. The global Healthcare Robotics Market is anticipated to flourish in the future by growing at a significantly higher CAGR.
This document discusses a proposed system called "Medical Store Automation" which aims to automate processes at medical stores to save time and effort. The key aspects of the proposed system include:
1. Automatically opening drawers containing requested medicines using an "automatic drawer opening system" to quickly locate items and reduce searching time.
2. Maintaining stock inventory electronically to always know medicine quantities available.
3. Updating medicine stock levels as items are sold to keep inventory information accurate.
The system is intended to reduce the burden on medical store workers and assist them in quickly finding and providing requested medicines to customers. It proposes using technologies like databases and Java programming to automate processes and inventory management.
This document provides guidance on risk assessment models used primarily for capital assessment purposes. It covers considerations for model design, implementation, validation, and governance. For model design, it discusses defining the model framework, integrating different risks, and designing stochastic models. For implementation, it addresses developing assumptions, using business data, IT requirements, and validation processes. Model validation involves conceptual and implementation checks. Governance involves defining roles and responsibilities, review processes, documentation standards, and compliance. The goal is to promote accuracy, comparability, consistency, transparency, reliability and practical implementation of risk assessment models.
This document summarizes an archived NIST technical publication on creating a patch and vulnerability management program from 2005. The publication has since been superseded by NIST Special Publication 800-40 Revision 3 from 2013.
The original 2005 publication provided guidance on establishing patch management programs and addressing legacy system needs. It covered topics such as developing a patch and vulnerability management process, creating a system inventory, monitoring for vulnerabilities and patches, prioritizing patch deployment, testing patches, and verifying systems have been patched.
The 2005 document was archived and superseded by the 2013 revision, which provides updated guidance for enterprise patch management technologies. The revision reflects the evolution of patching solutions and approaches over the intervening years.
This document provides an implementation guide for creating Personal Healthcare Monitoring Reports (PHMRs) using the Clinical Document Architecture Release 2 (CDA R2) standard. It defines constraints and requirements for the CDA header and sections. The guide is intended for use internationally. It was last updated in August 2010 as a second draft for trial use and comment. Feedback on the draft is requested.
The document describes a data model for representing clinical measurement terms and their relationships in a structured nomenclature. Key elements include base concepts, differentiating criteria sets to specialize concepts, and semantic links to define relationships between descriptive elements. The model supports building systematic names in a directed way and representing synonyms and language variations.
The document provides an overview of the Fennec UI, outlining its themes of maximizing screen space for content while minimizing typing. It then walks through the basic controls, navigation, notifications, add-ons/downloads/preferences, identity features, and desktop integration via Weave. Key aspects highlighted include finger-friendly design, quick lookup scenarios, and linking to the desktop Firefox experience.
The document discusses factors in interaction design for mobile experiences. It notes that while mobile browsing can be similar to stationary browsing, it is important to focus on how it is different. Some differences come from the mobile device itself, like small screens and direct manipulation interfaces, while other differences come from the user context of being mobile, interruptible, and having changing social and physical contexts. The document suggests designers consider the technical system, the user and their context, and the tasks users aim to complete.
Healthcare Robotics is a field that deals with combined medical & technological fields. Robots in healthcare are helping the medical personals for performing tasks that take lot of time & also making the medical process safer & more cost-effective. Healthcare Robotics is helpful for performing surgeries at small places & to handle risky substances. Healthcare Robotics finds a wide application is medical procedures, while some more technologies are under research. Use of robotics in Healthcare is increasing due to factors like; rise in number of elderly population, increase in number of minimally invasive surgical (MIS), rise in number of systems providing high resolution imaging, fine control & haptic feedback, reduction in treatment cost with increased quality, increase in technical advancement, severe shortage of medical personals, etc. Therefore, the Healthcare Robotics Market is anticipated to expand and has tremendous scope during the forecast period. The global Healthcare Robotics Market is anticipated to flourish in the future by growing at a significantly higher CAGR.
This document discusses a proposed system called "Medical Store Automation" which aims to automate processes at medical stores to save time and effort. The key aspects of the proposed system include:
1. Automatically opening drawers containing requested medicines using an "automatic drawer opening system" to quickly locate items and reduce searching time.
2. Maintaining stock inventory electronically to always know medicine quantities available.
3. Updating medicine stock levels as items are sold to keep inventory information accurate.
The system is intended to reduce the burden on medical store workers and assist them in quickly finding and providing requested medicines to customers. It proposes using technologies like databases and Java programming to automate processes and inventory management.
This document provides guidance on risk assessment models used primarily for capital assessment purposes. It covers considerations for model design, implementation, validation, and governance. For model design, it discusses defining the model framework, integrating different risks, and designing stochastic models. For implementation, it addresses developing assumptions, using business data, IT requirements, and validation processes. Model validation involves conceptual and implementation checks. Governance involves defining roles and responsibilities, review processes, documentation standards, and compliance. The goal is to promote accuracy, comparability, consistency, transparency, reliability and practical implementation of risk assessment models.
This document summarizes an archived NIST technical publication on creating a patch and vulnerability management program from 2005. The publication has since been superseded by NIST Special Publication 800-40 Revision 3 from 2013.
The original 2005 publication provided guidance on establishing patch management programs and addressing legacy system needs. It covered topics such as developing a patch and vulnerability management process, creating a system inventory, monitoring for vulnerabilities and patches, prioritizing patch deployment, testing patches, and verifying systems have been patched.
The 2005 document was archived and superseded by the 2013 revision, which provides updated guidance for enterprise patch management technologies. The revision reflects the evolution of patching solutions and approaches over the intervening years.
2010 OCDE Achieving Efficiency Improvements in the Health Sector through the ...Madrid Network
The document discusses how information and communication technologies (ICTs) can help drive improvements in healthcare quality and efficiency by enabling better care coordination, safer care through access to patient information and clinical guidelines, and more efficient chronic disease management. However, implementing ICTs in healthcare has proven difficult, with significant costs, delays, and failures experienced across OECD countries. The report analyzes case studies from several countries to identify conditions under which ICTs are most likely to achieve efficiency and quality gains in healthcare.
The document discusses how information and communication technologies (ICTs) can help drive improvements in healthcare quality and efficiency by enabling better care coordination, safer care through access to patient information and clinical guidelines, and more efficient chronic disease management. However, implementing ICTs in healthcare has proven difficult, with significant costs, delays, and failures experienced across countries. The report analyzes case studies from several OECD countries to identify conditions under which ICTs are most likely to achieve efficiency and quality gains in healthcare.
2010 OCDE Achieving Efficiency Improvements in the Health Sector through the ...guest4c3ea7
The document discusses how information and communication technologies (ICTs) can help drive improvements in healthcare quality and efficiency by enabling better care coordination, safer care through access to patient information and clinical guidelines, and more efficient chronic disease management. However, implementing ICTs in healthcare has proven difficult, with significant costs, delays, and failures experienced across countries. The report analyzes case studies from several OECD countries to identify conditions under which ICTs are most likely to achieve efficiency and quality gains in healthcare.
The global mobility-as-a-service market analysis by BIS Research projects the market to grow at a significant CAGR of 25.10% during the forecast period from 2020 to 2025.
Medical Simulation Market to Reach US$ 2.50 Billion by 2022Amy Williams
The medical simulation market is expected to reach $2.50 billion by 2022, growing at over 15% annually. Key drivers include technological innovation, demand for minimally invasive treatments, and focus on patient safety. The market is segmented by product/service, end user, and region. It includes simulation training services, software, anatomical models, and endovascular simulators used by hospitals, military, and academics for education. The report provides an overview, market analysis, company profiles of major players, and identifies new opportunities in the medical simulation industry.
This document provides a framework for an occupational health and safety (OH&S) management system. The purpose is to prevent work-related injury and illness and provide safe workplaces. Key aspects include leadership commitment, worker participation, hazard identification and risk assessment, compliance with legal requirements, OH&S objectives, and performance evaluation. Implementing the OH&S management system enables an organization to manage OH&S risks and improve performance over time. Success depends on factors such as leadership, communication, and resources to maintain the system.
Organ Preservation Market PPT: Demand, Trends and Business Opportunities 2022-27IMARC Group
Looking forward, the organ preservation market value is projected to reach a strong growth during the forecast period (2022-2027).
More info:- https://www.imarcgroup.com/organ-preservation-market
The IDMP Challenge - Whitepaper on ISO IDMP by CunesoftV E R A
The updated whitepaper on ISO IDMP - learn what you need to know during this transition. And how Cunesoft's cune-IDMP can help your organization: https://cunesoft.com/en/products/idmp/
Health Care System with Smart AssistantIRJET Journal
The document proposes a web-based health care system that incorporates a chatbot to allow patients to book appointments, receive health tips and predictions, and interact with doctors virtually. It describes the system architecture and modules for registration, appointment booking, health checkups, administrative functions, doctor functions, and patient functions. The system uses an SVM algorithm to classify data and aims to make healthcare more accessible and personalized through human-machine interaction.
HIS purchase projects in public hospitals of StyriaMiroslav Mađarić
This document summarizes the project to select and purchase a new hospital information system (HIS) for the KAGes public hospitals in Styria, Austria. It describes the multi-step evaluation process including requesting vendor information, product presentations, establishing test sites to evaluate the systems, visiting reference sites, and selecting finalists. Four vendors were selected for the final evaluation phase. Over 60 teams with 400 users and IT experts assessed the products over multiple sessions. Based on their recommendations, two vendors were selected for negotiations, and EDVg was ultimately chosen to implement their IS-H/IS-H*MED product in a new project called MEDOCS, with pilot installations beginning in 2000.
This document introduces the Disclosure Framework and Assessment Methodology referenced in the April 2012 CPSS-IOSCO report "Principles for Financial Market Infrastructures" (PFMI). The Disclosure Framework prescribes standard disclosures expected of FMIs to provide transparency. The Assessment Methodology provides guidance for assessing observance of the 24 principles and 5 responsibilities for authorities set forth in the PFMI. Together these documents support consistent implementation of the PFMI and promote transparency, objectivity and comparability of FMI assessments.
Medical Automation Technologies, Products and MarketsReportLinker.com
REPORT SCOPEINTRODUCTIONSTUDY BACKGROUNDSince the enactment of the Patient Protection and Affordable Care Act (PPACA) in 2010, the U.S. government and healthcare industry have stepped up their efforts to increase the efficiency of health care, with the twin objectives of containing costs and improving the quality of care. Information technology is at the forefront of this effort; indeed, BCC Research recently completed a study of healthcare IT technologies, products, and market opportunities (Report HLC048C).However, healthcare IT is just one segment of the broader field of medical automation, a field that many experts believe will revolutionize the way medical care is provided. Automated delivery of health care can contain costs, reduce errors, and improve outcomes.Major improvements in production efficiency and product quality have been demonstrated through automation in factories. Medical automation will borrow many of the principles developed in factory automation and apply them to the medical environment. Automation will have to demonstrate, however, that it is safe for patients, that it has more flexibility to accommodate the complex tasks within the hospital, and that it can generate a reasonable return on investment.GOALS AND OBJECTIVESThe report is an update of an earlier report published by BCC in 2009, and its goal is to identify and quantify the current and future market opportunities associated with medical automation. In support of this goal, here is a list of its specific objectives: * Identifying the medical automation technologies with the greatest commercial potential over the next 5 years (2011 to 2016). * Estimating the market for these technologies in 2010. * Analyzing the technical, economic, and other demand drivers for these products, and other prerequisites of success in these markets. * Projecting the potential U.S. markets for these technologies through 2016.INTENDED AUDIENCEThe report is intended especially for healthcare automation suppliers, as well as government agencies, healthcare policy analysts, and others seeking to understand the costs and preconditions for success of healthcare automation initiatives. Although the report is structured around specific technologies, it is largely nontechnical in nature. That is, it is concerned less with theory and jargon than with what works, how much of what works the market is likely to purchase, and at what price. As such, the report's main audience is composed of executive managers and marketing and financial analysts. It is not written specifically for scientists and technologists, although its findings are concerned with the markets for their work, including the availability of government and corporate research funding for different technologies, and applications that should interest them as well.SCOPE AND FORMATAs indicated above, medical automation is closely related to healthcare IT, which is the subject of a companion BCC report, HLC048C Healthcare Information Technology. However, for the purposes of this report, medical automation technologies are defined as technologies for the electromechanical control or operation of diagnostic or therapeutic processes or systems or training of healthcare professionals, which result in a reduced need or eliminate the need for human intervention. Examples of such medical automation technologies are listed: * Automated health assessment and monitoring technologies * Automated medical imaging and image analysis * Automated prescription fulfillment devices * Automated therapeutic (nonsurgical) devices * Robotic and computer-assisted surgical equipment * Automated laboratory testing and analysis * Automated healthcare logistics, resource, and patient tracking * Automated medical trainingThe study format includes the following major elements: * Executive summary * Definitions * Medical automation technologies and applications * Enabling technologies * End
MedTech Europe Code of Ethical Business PracticeMarket iT
This document outlines the MedTech Europe Code of Ethical Business Practice. It provides guidance for interactions between medical technology companies and healthcare professionals/organizations. Some key points:
- It aims to promote ethical standards while enabling innovation and education. Guidelines cover events, grants, research, consulting arrangements and more.
- Companies must comply with relevant laws and ensure transparency. Support cannot influence purchasing.
- For events, programs must relate to attendees' work and not include leisure. Location/venue cannot be the main attraction. Reasonable hospitality is allowed.
- Companies can support third party conferences and training. Grants and donations must be for genuine educational or research purposes. Consulting contracts must document legitimate work at fair market
IT Outsourcing (ITO) in the Life Sciences Industry - Service Provider LandscapeEverest Group
This report provides a comprehensive assessment of the service provider landscape for IT outsourcing (ITO) services in the life sciences industry. It maps 14 leading service providers on the Everest Group PEAK Matrix and includes detailed profiles of these service providers. This evaluation categorizes the service providers into Leaders, Major Contenders, and Emerging Players. It also identifies top three service providers as Star Performers, based on their year on year movement on the Matrix
Starting a new high-tech company is not easy. Furthermore, each experience is, by definition, unique. For example, the team behind the project, the problem which is
addressed, the technology upon which the solution is based, the business context when the start-up is being launched, etc. A high-tech start-up based on robotics technology is no different -- each project will be its own. However, despite all the individual characteristics of each new high-tech start-up, there are also basic elements which are common to virtually all entrepreneurial projects. Every project needs a business model. Every project needs a team to execute the model. Every project needs financing to develop its solution, and deliver it successfully to the marketplace.
This guide has as its objective to serve as a useful, practical reference, a document that can help lead a new project from the idea stage to a successfully launched high-tech start-up.
The key elements that are covered include the importance of high-tech start-ups to our economy and society, the specific opportunities and challenges of the robotics marketplace, characteristics of the right entrepreneur to lead the start-up, evaluating the technological position upon which the start-up is based, key considerations for defining a business model and business plan in order to convert the project from an idea to a successful company.
More info at http://www.tecnalia.com/en/industry-transport/index.htm
Organ Preservation Market PPT: Demand, Trends and Business Opportunities 2022-27IMARC Group
The global organ preservation market reached a value of US$ 163.5 Million in 2021. Looking forward, IMARC Group expects the market to reach US$ 242.6 Million by 2027, exhibiting at a CAGR of 6.8% during 2022-2027.
More info:- https://www.imarcgroup.com/organ-preservation-market
Situation Analysis on medical equipment in MaldivesRuby Med Plus
The document provides a situation analysis of capital and asset management of medical equipment in Maldivian health services. It finds that there is a lack of systematic planning, regulation, and assessment regarding the procurement, maintenance, and replacement of medical devices. Asset registers and capital planning are inadequate. There is no standard process for prioritizing funding requests and allocating capital budgets. Recommendations include developing asset management policies and procedures, standardized business cases for funding requests, multi-year capital plans by asset class, and guidelines for estimating medical equipment lifespan. Strengthening various departments involved in procurement, supply, and regulation of devices is also recommended.
Europe Organ Preservation Market PPT: Demand, Trends and Business Opportuniti...IMARC Group
The Europe organ preservation market size reached US$ 65.1 Million in 2022. Looking forward, IMARC Group expects the market to reach US$ 94.8 Million by 2028, exhibiting a growth rate (CAGR) of 6.34% during 2023-2028.
More Info:- https://www.imarcgroup.com/europe-organ-preservation-market
Orthopedic braces and Supports Market , Size, Share, Trends, Industry Scope 2...IMARC Group
According to the latest report by IMARC Group, that the global orthopedic braces and supports market size reached US$ 3.9 Billion in 2021. Orthopedic braces and supports are medical devices that alleviate chronic pain or temporary discomfort while recovering from a surgery or an athletic injury. They are made of rigid materials, such as hard plastics, soft materials such as spandex or other tightly knit fabrics, designed to inhibit the movement of a joint.
This document provides an overview of clinical engineering principles as taught by Prof. Bassel Tawfik at Cairo University in 2018. It discusses healthcare delivery systems and major stakeholders. It also defines clinical engineering and its scope of work, which includes medical equipment planning during hospital design, as well as equipment operation through testing, calibration, maintenance and management. The document outlines hospital departments and functions, including administration, medico-surgical services, and support services. It also covers the hospital and medical equipment lifecycles.
Este documento presenta un estudio sobre la aplicación de Big Data en salud digital realizado por equipos de trabajo de la Fundación Vodafone España y Red.es. El estudio analiza el marco conceptual de Big Data y salud digital, sus aplicaciones actuales y futuras, los beneficios potenciales, y las barreras a superar para su implantación. El objetivo es comprender cómo Big Data puede ayudar a mejorar la salud y calidad de vida de los ciudadanos.
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More info:- https://www.imarcgroup.com/organ-preservation-market
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Starting a new high-tech company is not easy. Furthermore, each experience is, by definition, unique. For example, the team behind the project, the problem which is
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Orthopedic braces and Supports Market , Size, Share, Trends, Industry Scope 2...IMARC Group
According to the latest report by IMARC Group, that the global orthopedic braces and supports market size reached US$ 3.9 Billion in 2021. Orthopedic braces and supports are medical devices that alleviate chronic pain or temporary discomfort while recovering from a surgery or an athletic injury. They are made of rigid materials, such as hard plastics, soft materials such as spandex or other tightly knit fabrics, designed to inhibit the movement of a joint.
This document provides an overview of clinical engineering principles as taught by Prof. Bassel Tawfik at Cairo University in 2018. It discusses healthcare delivery systems and major stakeholders. It also defines clinical engineering and its scope of work, which includes medical equipment planning during hospital design, as well as equipment operation through testing, calibration, maintenance and management. The document outlines hospital departments and functions, including administration, medico-surgical services, and support services. It also covers the hospital and medical equipment lifecycles.
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Este documento presenta un estudio sobre la aplicación de Big Data en salud digital realizado por equipos de trabajo de la Fundación Vodafone España y Red.es. El estudio analiza el marco conceptual de Big Data y salud digital, sus aplicaciones actuales y futuras, los beneficios potenciales, y las barreras a superar para su implantación. El objetivo es comprender cómo Big Data puede ayudar a mejorar la salud y calidad de vida de los ciudadanos.
La evolución de HL7 para IoT y sus propuestas de interoperabilidad.
FHIR como estandard para la interoperabilidad del IoT.
Como IoT en salud todavía tiene áreas para desarrollar y HL7 puede dar respuesta a la interoperabilidad de los diferentes dispositivos IoT conectados
El documento describe la construcción de un canal personal de salud para los ciudadanos que proporcionará acceso seguro a su historia clínica electrónica y nuevos servicios de empoderamiento del paciente. Se basará en principios comunes de interoperabilidad, disponibilidad, seguridad y privacidad de datos para permitir la integración de nuevas fuentes de información como dispositivos médicos.
El documento trata sobre la integración de dispositivos móviles en el campo de la salud (mHEALTH). Describe tres servicios principales relacionados con mHEALTH: servicios para profesionales, servicios para proveedores de salud y servicios para ciudadanos. También discute varios marcos y estándares clave como FHIR y hDATA que permiten el intercambio y almacenamiento seguros de datos médicos a través de dispositivos móviles y la nube.
The document summarizes the 2013 activities of HL7 Spain including their annual plenary meeting in September in Cambridge, MA. It discusses HL7 Spain's membership which includes 45 healthcare industry members, 16 administration members, and 4 faculty members. It also outlines HL7 Spain's training program which had 223 attendees in 2013 and their certification program which certified 24 new professionals.
El documento describe el proyecto Diccionario Clínico para iSalut, cuyo objetivo es normalizar el vocabulario del Sistema Sanitario Integrado de Cataluña (SISCAT) utilizando SNOMED CT como terminología de referencia. SNOMED CT permitirá representar de forma homogénea el contenido de los documentos clínicos y garantizar la interoperabilidad semántica entre agentes del SISCAT y a nivel internacional. El Diccionario Clínico definirá de forma estandarizada el vocabulario por dominios prioriz
HL7 Spain es una asociación sin fines de lucro que promueve los estándares HL7 para lograr la interoperabilidad de los sistemas de información de salud en España. La interoperabilidad permite que estos sistemas compartan y usen información de forma conjunta para mejorar la atención al paciente. España ha adoptado los estándares HL7 y ha logrado casos exitosos de interoperabilidad como la historia clínica electrónica y la receta electrónica en varias regiones. HL7 Spain continuará colaborando para expandir el uso de estándares
Este documento presenta un modelo funcional para un sistema de historia de salud personal (PHR-S) conforme a las normas de HL7 Spain. Describe los componentes y conceptos clave del modelo, incluyendo diferentes enfoques de desarrollo como uno orientado al proveedor de salud. Luego proporciona un catálogo detallado de funciones para un PHR orientado al proveedor, organizadas en secciones como perfil del usuario, gestión de datos clínicos, bienestar y autocuidado, y gestión de consultas médicas. El objetivo es defin
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BPMN 2.0 es un estándar para la modelización de procesos de negocio. Ofrece elementos para modelar actividades, eventos, flujos de trabajo y participantes. Las comunicaciones definen conjuntos de mensajes intercambiados entre participantes. Las tareas representan unidades de trabajo y los subprocesos permiten refinar actividades. Las transacciones agrupan conjuntos de actividades que se ejecutan como una unidad atómica.
El documento describe el proyecto EPSOS, que busca establecer la interoperabilidad de los sistemas de información sanitaria entre 12 países europeos. El objetivo es demostrar la interoperabilidad transfronteriza a través del resumen clínico y la receta electrónica. El proyecto se inició en 2009 y utiliza perfiles IHE como marco para lograr la interoperabilidad técnica y semántica.
El documento describe los beneficios de una historia clínica digital normalizada, incluyendo su uso para la asistencia clínica, docencia, investigación, epidemiología y mejora de la calidad. Señala la necesidad de desarrollar nuevos servicios como la continuidad asistencial y la telemedicina utilizando las TIC. Explica que estructurar y representar el conocimiento clínico mediante un vocabulario controlado como SNOMED CT permite traducir, obtener información y aplicar reglas. Concluye que se deben centrar los esfuerzos