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...
| Autors principals: | , |
|---|---|
| Format: | Journal article |
| Idioma: | English |
| Publicat: |
Mark Allen Healthcare
2023
|