Overview of the US FDA medical device approval process.

Abstract:

:Increasing barriers to medical device innovation in the United States including constrained financial resources and rising research costs require that physicians take on greater involvement in medical device development, evaluation, and regulatory processes. Such involvement requires that physicians understand basic aspects of the regulatory process for medical devices and recognize the myriad opportunities for involvement in these activities.

journal_name

Curr Cardiol Rep

authors

Sastry A

doi

10.1007/s11886-014-0494-3

subject

Has Abstract

pub_date

2014-01-01 00:00:00

pages

494

issue

6

eissn

1523-3782

issn

1534-3170

journal_volume

16

pub_type

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