Assessment of medical device regulator COVID-19 policies on entry to market for prioritised devices: a case study
<strong>Background/Aims<br></strong> In response to the COVID-19 pandemic, medical devices were given exceptional use authorisations. Medical device regulators around the world modified their administrative approach to medical device approval to ensure that relevant devices and per...
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| Médium: | Journal article |
| Jazyk: | English |
| Vydáno: |
Mark Allen Healthcare
2023
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