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- In vitro diagnostics - Global
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
- In vitro diagnostics - 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
- Week of Quality for In Vitro Diagnostics 2025: Registration Now Open
Join us for the WHO's Week of Quality for IVDs training program Register your interest to participate in this valuable training program IVD manufacturers and regulatory authorities (Ministry of Health, National Regulatory Authorities) in all WHO regions are welcome to attend
- Call for experts: Strategic Advisory Group of Experts on In Vitro . . .
SAGE IVD members are appointed for 2 years and can be reappointed once Functions of the Strategic Advisory Group of Experts on In Vitro DiagnosticsTo serve as a principal advisory group to the WHO Director-General on all aspects of IVDs
- WHO approves first mpox diagnostic test for emergency use, boosting . . .
The World Health Organization (WHO) has listed the first mpox in vitro diagnostic (IVD) under its Emergency Use Listing (EUL) procedure, an important step in improving global access to mpox testing
- Health products policy and standards
The World Health Organization (WHO) has established a Strategic Advisory Group of Experts on In Vitro Diagnostics (SAGE IVD) to act as an advisory body on matters of global policies and strategies related to in vitro diagnostics (IVDs)
- Strategic Advisory Group of Experts on In Vitro Diagnostics (SAGE IVD)
In 2018, the World Health Organization (WHO) established the Strategic Advisory Group of Experts on In Vitro Diagnostics (SAGE IVD) to act as an advisory body to matters of global policies and strategies related to in vitro diagnostics (IVDs)
- In vitro diagnostics for COVID-19 - World Health Organization (WHO)
The EUL procedure is developed to expedite the availability of IVDs needed in public health emergency situations It is intended to assist interested procurement agencies and Member States on the suitability for use of a specific IVD, based on a minimum set of available quality, safety, and performance data
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