Understanding Variation Among Medical Device Reporting Sources: A Study of the MAUDE Database.
PMID : 39516116 ·
M, e, i, t, a, l, , M, i, s, h, a, l, i, ;, , N, a, d, a, v, , S, h, e, f, f, e, r, ;, , O, r, e, n, , M, i, s, h, a, l, i, ;, , M, a, y, a, , N, e, g, e, v
Publicité
Résumé
Increasing medical device usage raises concerns regarding unexpected, potentially life-threatening events that pose public health risks. Such events are reported to the Food and Drug Administration (FDA), and cataloged in the Manufacturer and User Facility Device Experience (MAUDE) database, a vital tool for post market surveillance that requires information of high quality and integrity, particularly concerning reporting sources. To analyze reporting behavior among different reporters, includin
Publicité
Source officielle
Voir sur PubMed →Données issues de PubMed / NCBI. Pour le texte intégral et les informations les plus récentes, consultez toujours la notice officielle.