|
IMDRF to Focus Initially on UDI, e-Submissions ‘Table of Contents’
Early goals of the newly formed International Medical Device Regulators Forum (IMDRF) include defining a common international “table of contents” for electronic submissions and designing a roadmap for implementation of a unique device identification system.
This article is viewable by subscribers only. To view this article, please select an option below.
|
Related Articles
|
Subscribe
Archives