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- Diagnostics - Global - World Health Organization (WHO)
Diagnostics are the most important tools that empower the health workforce in the identification of diseases or health conditions They allow the initiation of treatments in order to avoid further complications and costly treatments for patients
- In vitro diagnostics - Global - World Health Organization (WHO)
In vitro diagnostics (IVDs) are tests that can detect disease, conditions and infections In vitro simply means ‘in glass’, meaning these tests are typically conducted in test tubes and similar equipment, as opposed to in vivo tests, which are conducted in the body itself
- Strengthening diagnostics capacity - World Health Organization (WHO)
In response, WHO established the Diagnostics Taskforce as a collaborative mechanism between all WHO programmes, at all three levels of the organization, to support the implementation of the resolution, and to serve as the entry point to all stakeholders working with countries on strengthening diagnostics capacity Taskforce members support
- WHO publishes new Essential Diagnostics List and urges countries to . . .
To address the lack of access to tests and testing services in multiple countries, WHO since 2018 has published a yearly essential diagnostics list (EDL), a basket of recommended in vitro diagnostics that should be available at point-of-care and in laboratories in all countries to increase timely and life-saving diagnoses The latest edition, published today, includes WHO-recommended COVID-19
- Diagnostic testing for SARS-CoV-2
This document provides interim guidance to laboratories and other stakeholders involved in diagnostics for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) It covers the main considerations for specimen collection, nucleic acid amplification testing (NAAT), antigen (Ag), antibody (Ab) detection and quality assurance This document will be updated as new information becomes
- Guidance for post-market surveillance and market surveillance of . . .
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
- 2. 2 Diagnostic testing for TB - World Health Organization (WHO)
In general in 2022, levels of bacteriological confirmation were highest in high-income countries (median, 89%), where there is wide access to the most sensitive diagnostic tests, and lowest in low-income countries (median, 71%) (Fig 2 2 3) Over-reliance on direct sputum smear microscopy is inherently associated with a relatively high proportion of pulmonary TB cases that are clinically
- WHO standard: universal access to rapid tuberculosis diagnostics
The WHO standard: Universal access to rapid tuberculosis diagnostics sets benchmarks to achieve universal access to WHO-recommended rapid diagnostics (WRDs), increase bacteriologically confirmed tuberculosis and drug resistance detection, and reduce the time to diagnosis WHO-recommended rapid diagnostics are highly accurate, cost-effective, reduce the time to treatment initiation, and impact
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