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29 Ιαν 2021 · The latest edition, published today, includes WHO-recommended COVID-19 tests (PCR and Antigen), expands the suite of tests for vaccine-preventable and infectious diseases and non-communicable diseases (such as cancer and diabetes), and introduces a section on endocrinology, which is important for reproductive and women’s health.
- En Anglais
This document provides interim guidance to laboratories and...
- En Anglais
WHO works with Member States, collaborating centres, partners and expert groups to develop and revise guidelines and tools, including norms and standards of all types of diagnostics (in vitro and in vivo). WHO selects priority medical devices required for multiple diseases and health conditions.
11 Σεπ 2020 · 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.
A Medical Laboratory Scientist (MLS) or Clinical Laboratory Scientist (CLS) or Medical Technologist (MT) is a licensed Healthcare professional who performs diagnostic testing of body fluids, blood and other body tissue. The Medical Technologist is tasked with releasing the patient results to aid in further treatment.
29 Δεκ 2015 · The committee uses the term “diagnostic testing” to be inclusive of all types of testing, including medical imaging, anatomic pathology, and laboratory medicine, as well as other types of testing, such as mental health assessments, vision and hearing testing, and neurocognitive testing.
1 Σεπ 2020 · Molecular diagnostic tests are driving most of infectious disease testing in the 21st Century 1 and include increasingly complex test menus, individual molecular analyses, as well as point-of-care testing options.
We have identified six steps that must be addressed when selecting an in vitro diagnostic test: (i) define the test’s purpose; (ii) review the market and check each product’s specification; (iii) review the test’s regulatory approval; (iv) obtain data on the diagnostic accu-racy of the test under ideal conditions.
