Medical devices - World Health Organization (WHO)
Jun 16, 2024 · The "Medical Devices Technical Series (MDTS)" is a series of publications intended to increase access to medical devices. WHO developed this series that cover the following areas: Development of medical devices policies. Human resources for medical devices. Regulation of medical devices.
Medical devices - World Health Organization (WHO)
Apr 6, 2011 · Health products policy and standards. Our team provides authoritative guidance and standards on quality, safety and efficacy of health products and supports countries to formulate evidence-based policies and ensure good practice throughout the value chain. Assistive Technology. Medical devices. Essential Medicines.
Nomenclature of medical devices - World Health Organization …
The nomenclature of medical devices is a coding and naming system used to generically classify and identify all medical devices and related health products. According to different classification and nomenclature systems, there are between 5,000 to 24,000 different types of medical devices. They range from the very simple to complex, inexpensive ...
In vitro diagnostics - Global - World Health Organization (WHO)
Feb 10, 2020 · More. 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 tests may be done in laboratories, health care ...
Management and Safe Use of Medical Devices - World Health …
Medical devices should be safe, of good quality and appropriate to the settings in where they are used. Recognizing this important role of health technologies towards universal health coverage, the World Health Assembly adopted resolution WHA60.29 in May 2007. By adopting this resolution, Member States urged expansion of expertise in the field ...
Health products policy and standards - World Health Organization …
The 67th WHA approved the resolution “Regulatory system strengthening for medical products." It states the importance of regulations for medical devices as one of the medical products, for better public health outcome and to increase access to safe, effective and quality medical products. The complete text of the Resolution, in the 6 WHO ...
Global atlas of medical devices - World Health Organization (WHO)
Nov 25, 2022 · Health products policy and standards. Our team provides authoritative guidance and standards on quality, safety and efficacy of health products and supports countries to formulate evidence-based policies and ensure good practice throughout the value chain. < Back to Medical devices. Global atlas of medical devices.
Guidance for post-market surveillance and market surveillance of ...
Jun 20, 2021 · 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 …
121 used together with a particular IVD medical device to enable or assist that device to 122 be used in accordance with its intended use. 123 Note: Some jurisdictions include accessories to a medical device and accessories to 124 an IVD medical device within their definitions of medical device or IVD medical 125 device, respectively. Other ...
Health products policy and standards - World Health Organization …
Health products policy and standards. Our team provides authoritative guidance and standards on quality, safety and efficacy of health products and supports countries to formulate evidence-based policies and ensure good practice throughout the value chain. < …