The US Food and Drug
Administration (FDA) has proposed
a new program for early access
to high-risk medical devices for
patients with serious conditions
whose medical needs are unmet by
current technology.
Called the Expedited Access
Premarket Approval Application
(Expedited PMA), it had earlier and
more interaction with FDA staff, the
organisation said.
For more, CLICK HERE.The above article was sent to subscribers in Pharmacy Daily's issue from 23 Apr 14 To see the full newsletter, see the embedded issue below or CLICK HERE to download Pharmacy Daily from 23 Apr 14
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