Aviso: Este sitio agrega datos públicos oficiales de la FDA, ClinicalTrials.gov, PubMed y SEC EDGAR solo como referencia general. No constituye asesoramiento médico, diagnóstico, recomendaciones de tratamiento ni asesoramiento de inversión.

PubMed

Patient-reported outcomes and medical device evaluation: from conception to implementation.

PMID: 35608682 ·

C, h, r, i, s, t, i, n, a, , M, , W, e, b, b, e, r, ;, , B, r, i, t, t, a, n, y, , C, a, l, d, w, e, l, l, ;, , F, r, a, s, e, r, , D, , B, o, c, e, l, l, ;, , A, n, i, n, d, i, t, a, , S, a, h, a, ;, , M, i, c, h, e, l, l, e, , E, , T, a, r, v, e, r

RevistaJournal of patient-reported outcomes
Año
PMID35608682

Resumen

The insights gleaned from patient-reported outcomes (PROs) have implications across the healthcare ecosystem, from clinical investigations to evaluate the safety and effectiveness of medical devices to clinical care and reimbursement decisions. The U.S. Food and Drug Administration's (FDA) Center for Devices and Radiological Health (CDRH) hosted a public meeting in September 2020 discussing how PROs can be used in medical device evaluation throughout the total product life cycle, as well as meth

Fuente oficial

Ver en PubMed →

Datos obtenidos de PubMed / NCBI. Para consultar el texto completo y la información más reciente, remítase siempre al registro oficial.

↑