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Individuals can use m-health to access resource materials on health issues. (...) oec-match=&oec- category=22&Search.x=13&Search.y=16 Product Description Patient Keeper offers a comprehensive collection of software, handheld devices and accessories for mobile health care professionals. (...) PatientKeeper eSignature is a software product that provides for fast, accurate electronic signing on mobile devices, such as PDAs. In most instances when a health care provider enters a clinical note on a PDA, in order for it to be a part of the official medical record, it must be reviewed, edited, and signed.
Language:English
Score: 961235.4 - https://publicadministration.u...%20ICT%20Apps%20Volume%20I.pdf
Data Source: un
"The Institute for Public Health of FBiH, in cooperation with the cantonal public health institutes, carried out a needs assessment and defined a list of locations for installing LCD devices. (...) Aida Ramić Čatak, pomoćnica direktora Zavoda za javno zdravstvo FBiH za stručne poslove By procuring 20 LCD devices, UNICEF BiH wants to support alternative methods of communication with the community in order to convey important information about public health.  (...) Fatima Čengić, Head of the Health and ECD Programmes at UNICEF BiH. Fatima Čengić, voditeljica Programa za zdravstvo i za rani rast i razvoj u UNICEF BiH The healthcare facilities and institutions to which the LCD devices were donated thanked UNICEF BiH and the Institute for Public Health of the Federation of BiH for the valuable donation.
Language:English
Score: 960980.4 - https://www.unicef.org/bih/en/...cilities-and-institutions-fbih
Data Source: un
Recent appearance of various portable bio-sensor based analytic devices, wearable health monitoring devices and connectability of these devices through UWB to servers will make it possible to fuse those health monitoring devices and home-network technology. This combination of home network technology and portable devices provides us unlimited possibilities of future e- Health applications. (...) This presentation will discuss business scenarios of future e-Health and its need of standards.
Language:English
Score: 960669.9 - https://www.itu.int/ITU-T/work...tworking/abstracts/s3-kwak.pdf
Data Source: un
Select language Select language English العربية 中文 Français Русский Español Home Health Topics All topics » A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Resources » Fact sheets Facts in pictures Multimedia Publications Questions & answers Tools and toolkits Popular » Air pollution Coronavirus disease (COVID-19) Hepatitis Monkeypox Countries All countries » A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Regions » Africa Americas South-East Asia Europe Eastern Mediterranean Western Pacific WHO in countries » Statistics Cooperation strategies Ukraine emergency Newsroom All news » News releases Statements Campaigns Commentaries Events Feature stories Speeches Spotlights Newsletters Photo library Media distribution list Headlines » Emergencies Focus on » Afghanistan crisis COVID-19 pandemic Northern Ethiopia crisis Syria crisis Ukraine emergency Monkeypox outbreak Greater Horn of Africa crisis Latest » Disease Outbreak News Travel advice Situation reports Weekly Epidemiological Record WHO in emergencies » Surveillance Research Funding Partners Operations Independent Oversight and Advisory Committee Data Data at WHO » Global Health Estimates Health SDGs Mortality Database Data collections Dashboards » COVID-19 Dashboard Triple Billion Dashboard Health Inequality Monitor Highlights » Global Health Observatory SCORE Insights and visualizations Data collection tools Reports » World Health Statistics 2022 COVID excess deaths DDI IN FOCUS: 2022 About WHO About WHO » People Teams Structure Partnerships and collaboration Collaborating centres Networks, committees and advisory groups Transformation Our Work » General Programme of Work WHO Academy Activities Initiatives Funding » Investment case WHO Foundation Accountability » Audit Budget Financial statements Programme Budget Portal Results Report Governance » World Health Assembly Executive Board Election of Director-General Governing Bodies website Home / Publications detail / Guidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostics Guidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostics 20 June 2021  |  Publication Download (2.3 MB) Overview Post-market surveillance is a set of activities conducted by manufacturers, to collect and evaluate  experience gained from medical devices that have been placed on the market, and to identify the need  to take any action. Post-market surveillance is a crucial tool to ensure that medical devices continue to  be safe and well-performing and to ensure actions are undertaken if the risk of continued use of the  medical device outweighs the benefit. (...) Other languages: Russian Chinese Arabic WHO Team Access to Assistive Technology and Medical Devices, Access to Medicines and Health Products , Health Product Policy and Standards , Incidents and SF , Medical Devices and Diagnostics, Regulation and Prequalification , Regulation and safety Editors World Health Organization Number of pages 86 Reference numbers ISBN: 978-92-4-001531-9 Copyright Regions Africa Americas Eastern Mediterranean Europe South-East Asia Western Pacific Policies Cyber security Ethics Permissions and licensing Preventing sexual exploitation Terms of use About us Careers Library Procurement Publications Frequently asked questions Contact us Subscribe to our newsletters Privacy Legal Notice © 2022 WHO
Language:English
Score: 960171 - https://www.who.int/publicatio...-detail-redirect/9789240015319
Data Source: un
Select language Select language English العربية 中文 Français Русский Español Português Home Health Topics All topics » A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Resources » Fact sheets Facts in pictures Multimedia Publications Questions & answers Tools and toolkits Popular » Air pollution Coronavirus disease (COVID-19) Hepatitis Monkeypox Countries All countries » A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Regions » Africa Americas South-East Asia Europe Eastern Mediterranean Western Pacific WHO in countries » Statistics Cooperation strategies Ukraine emergency Newsroom All news » News releases Statements Campaigns Commentaries Events Feature stories Speeches Spotlights Newsletters Photo library Media distribution list Headlines » Emergencies Focus on » Afghanistan crisis COVID-19 pandemic Northern Ethiopia crisis Syria crisis Ukraine emergency Monkeypox outbreak Greater Horn of Africa crisis Latest » Disease Outbreak News Travel advice Situation reports Weekly Epidemiological Record WHO in emergencies » Surveillance Research Funding Partners Operations Independent Oversight and Advisory Committee Data Data at WHO » Global Health Estimates Health SDGs Mortality Database Data collections Dashboards » COVID-19 Dashboard Triple Billion Dashboard Health Inequality Monitor Highlights » Global Health Observatory SCORE Insights and visualizations Data collection tools Reports » World Health Statistics 2022 COVID excess deaths DDI IN FOCUS: 2022 About WHO About WHO » People Teams Structure Partnerships and collaboration Collaborating centres Networks, committees and advisory groups Transformation Our Work » General Programme of Work WHO Academy Activities Initiatives Funding » Investment case WHO Foundation Accountability » Audit Budget Financial statements Programme Budget Portal Results Report Governance » World Health Assembly Executive Board Election of Director-General Governing Bodies website Home / Publications / i / item / Guidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostics - Select language - العربية 中文 français русский español português Guidance for post-market surveillance and market surveillance of medical devices, including in vitro diagnostics 20 June 2021  |  Publication Download (2.3 MB) Overview Post-market surveillance is a set of activities conducted by manufacturers, to collect and evaluate  experience gained from medical devices that have been placed on the market, and to identify the need  to take any action. Post-market surveillance is a crucial tool to ensure that medical devices continue to  be safe and well-performing and to ensure actions are undertaken if the risk of continued use of the  medical device outweighs the benefit. (...) Other languages: Russian Chinese Arabic WHO Team Access to Assistive Technology and Medical Devices, Access to Medicines and Health Products , Health Product Policy and Standards , Incidents and SF , Medical Devices and Diagnostics, Regulation and Prequalification , Regulation and safety Editors World Health Organization Number of pages 86 Reference numbers ISBN: 978-92-4-001531-9 Copyright Regions Africa Americas Eastern Mediterranean Europe South-East Asia Western Pacific Policies Cyber security Ethics Permissions and licensing Preventing sexual exploitation Terms of use About us Careers Library Procurement Publications Frequently asked questions Contact us Subscribe to our newsletters Privacy Legal Notice © 2022 WHO
Language:English
Score: 960171 - https://www.who.int/publications/i/item/9789240015319
Data Source: un
Availing healthcare in the health and m-health applications have huge potential. (...) Two such ICT access standards are the (GOe) defines m-health as “medical and public health 3GPP-based 5G technology and IEEE-based Wi-Fi 6. practice supported by mobile devices, such as mobile phones, However, challenges exist in the ecosystem that inhibit the patient monitoring devices, personal digital assistants realization of the full potential of these technologies. (...) The government, for take place, the end devices can become more sophisticated instance, must make decisions of allotting resources to other including equipment for remote surgery and real-time pressing needs and rural health often does not get the 978-92-61-28401-5/CFP1968P-ART @ ITU 2019 – 23 – Kaleidoscope     38     39     40     41     42     43     44     45     46     47     48          
Language:English
Score: 959165.1 - https://www.itu.int/en/publica...e/files/basic-html/page43.html
Data Source: un
It is based on a similar publication issued by the Pan American Health Organization (PAHO) in 1999 that reviewed the Canadian Medical Devices Regulatory System. (...) Lepakhin Assistant Director-General Health Technology and Pharmaceuticals Glossary vii Note on the definition of medical devices The term “medical devices” includes everything from highly sophisticated computerized medical equipment down to simple wooden tongue depressors. (...) In practice, risk assessment of medical devices is based on the experience of health care professionals and on safety design engineering.
Language:English
Score: 958707.4 - https://www.who.int/medical_de...ications/en/MD_Regulations.pdf
Data Source: un
Patients are usually not very familiar with the services offered by different hospitals, they can usually just logon to the e-Health centre's portal and access services, whereas the e-Health centre is usually familiar and can determine the target hospitals based on their professional knowledge. (...) In other words, when the devices on a patient report data to the e-Health centre, the centre can intelligently help the patient to select the best target hospitals and route the data to those hospitals for joint diagnosis. (...) In this case, the devices should be interoperable with existing systems (e.g., data format, service capabilities invocation, etc.), that is the e-Health system should be able to collaborate and inter-work with the existing application systems which are usually heterogeneous. – Traffic load balancing should be taken into consideration in order to cope with particular situations.
Language:English
Score: 958015.6 - https://www.itu.int/en/publica.../files/basic-html/page303.html
Data Source: un
Priority medical devices list for the COVID-19 response and associated technical specifications World Health Organization Global Regions World Health Organization WHO Regional websites When autocomplete results are available use up and down arrows to review and enter to select. (...) It is intended for policy-makers and planning officers in Ministries of Health, procurement and regulatory agencies, intergovernmental and international agencies as well as the medical device industry.  (...) DOWNLOAD HERE WHO Team Access to Assistive Technology and Medical Devices, Health Product Policy and Standards , Medical Devices and Diagnostics, WHO Headquarters (HQ) Number of pages 176 Reference numbers WHO Reference Number: WHO/2019-nCoV/MedDev/TS/O2T.V2 Copyright Regions Africa Americas Eastern Mediterranean Europe South-East Asia Western Pacific Policies Cyber security Ethics Permissions and licensing Preventing sexual exploitation Terms of use About us Careers Library Procurement Publications Frequently asked questions Contact us Subscribe to our newsletters Privacy Legal Notice © 2022 WHO
Language:English
Score: 957977 - https://www.who.int/publicatio...WHO-2019-nCoV-MedDev-TS-O2T.V2
Data Source: un
Interagency List of Priority Medical Devices for Essential Interventions for Reproductive, Maternal, Newborn and Child Health Global Regions WHO Regional websites Africa Americas South-East Asia Europe Eastern Mediterranean Western Pacific When autocomplete results are available use up and down arrows to review and enter to select. (...) The medical devices are allocated across the reproductive, maternal, newborn and child health continuum of care according to the level of health-care delivery. WHO Team Access to Assistive Technology and Medical Devices, Access to Medicines and Health Products , Health Product Policy and Standards , Maternal, Newborn, Child & Adolescent Health & Ageing , Medical Devices and Diagnostics Editors WHO, UNFPA, UNICEF Number of pages 116 Reference numbers ISBN: 9789241565028 Copyright World Health Organization - All rights reserved Regions Africa Americas Eastern Mediterranean Europe South-East Asia Western Pacific Policies Cyber security Ethics Permissions and licensing Preventing sexual exploitation Terms of use About us Careers Library Procurement Publications Frequently asked questions Contact us Subscribe to our newsletters Privacy Legal Notice © 2022 WHO
Language:English
Score: 957139.7 - https://www.who.int/publicatio...-detail-redirect/9789241565028
Data Source: un