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- Title
WHO Global Model Regulatory Framework for medical devices including in vitro diagnostic medical devices: WHO Medical device technical series Replacement of Annex 4 of WHO Technical Report Series, No. 1003.
- Abstract
The article focuses on the importance of regulating medical devices, including in vitro diagnostics, to ensure their quality, safety, and performance. It highlights the World Health Organization (WHO) efforts to provide support to countries in developing or revising their national regulatory controls for medical devices. It reports rapid advancements in technology, evolving usage settings, and the need for equitable access to reliable medical devices, especially during the COVID-19 pandemic.
- Subjects
MEDICAL equipment; MEDICAL software; TECHNICAL reports; DISPOSABLE medical devices; ELECTRONIC waste; SPARE parts; MARIJUANA growing
- Publication
WHO Technical Report Series, 2023, Issue 1045, p179
- ISSN
0512-3054
- Publication type
Article