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PubMed

Medical Device Regulation: A Comparison of the United States and the European Union.

PMID: 27195383 · 2016

T, r, a, v, i, s, , G, , M, a, a, k, ;, , J, a, m, e, s, , D, , W, y, l, i, e

RevistaThe Journal of the American Academy of Orthopaedic Surgeons
Ano2016
PMID27195383

Resumo

Medical device regulation is a controversial topic in both the United States and the European Union. Many physicians and innovators in the United States cite a restrictive US FDA regulatory process as the reason for earlier and more rapid clinical advances in Europe. The FDA approval process mandates that a device be proved efficacious compared with a control or be substantially equivalent to a predicate device, whereas the European Union approval process mandates that the device perform its int

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