The Impact of COVID-19 on Medical Device Reporting and Investigation
IntroductionThe Manufacturer and User Facility Device Experience (MAUDE) database houses medical device reports submitted to the U.S. Food and Drug Administration (FDA). In May 2020, the FDA released guidance about medical device reporting during a pandemic, anticipating delays in reporting and inve...
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| Egile Nagusiak: | , , , , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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Patient Safety Authority
2021-09-01
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| Saila: | Patient Safety |
| Sarrera elektronikoa: | https://doi.org/10.33940/data/2021.9.3 |
| Etiketak: |
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