Medical device similarity analysis: a promising approach to medical device equivalence regulation.
PMID : 39300713 ·
J, a, n, , S, ü, n, d, e, r, m, a, n, n, ;, , J, o, a, q, u, i, n, , D, e, l, g, a, d, o, , F, e, r, n, a, n, d, e, z, ;, , R, u, p, e, r, t, , K, e, l, l, n, e, r, ;, , T, h, e, o, d, o, r, , D, o, l, l, ;, , U, l, r, i, c, h, , P, , F, r, o, r, i, e, p, ;, , A, n, n, e, t, t, e, , B, i, t, s, c, h
Publicité
Résumé
This study aims to facilitate the identification of similar devices for both, the European Medical Device Regulation (MDR) and the US 510(k) equivalence pathway by leveraging existing data. Both are related to the regulatory pathway of read across for chemicals, where toxicological data from a known substance is transferred to one under investigation, as they aim to streamline the accreditation process for new devices and chemicals. This study employs latent semantic analysis to generate similar
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.