Reporting of Death in US Food and Drug Administration Medical Device Adverse Event Reports in Categories Other Than Death

IMPORTANCE: In the US, most postmarket medical device safety data are obtained through adverse event reports that are submitted to the US Food and Drug Administration (FDA)’s Manufacturer and User Facility Device Experience (MAUDE) database. Adverse event reports are classified by the reporter as in...

Celý popis

Uloženo v:
Podrobná bibliografie
Vydáno v:JAMA Intern Med
Hlavní autoři: Lalani, Christina, Kunwar, Elysha M., Kinard, Madris, Dhruva, Sanket S., Redberg, Rita F.
Médium: Artigo
Jazyk:Inglês
Vydáno: American Medical Association 2021
Témata:
Original Investigation
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC8314174/
https://ncbi.nlm.nih.gov/pubmed/34309624
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamainternmed.2021.3942
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky