Generics BulletinHBW InsightIn VivoMedtech InsightPink SheetScrip

Generics Bulletin

Medtech Insight

'Breakthrough' Blueprint: US FDA Draft Guideline Outlines Revised Expedited Development Program

Oct 24 2017

• By David Filmore

Light bulb in a blue print

Related Content

US FDA Ready To Accept 510(k) Devices To Expedited Access/Breakthrough Pathway

May 08 2017

FDA 'Cures' Fund Breakdown: Breakthrough Devices, HDEs, IRB Flexibility And More

May 09 2017

MDUFA IV Makeover For US FDA Guidances

Oct 03 2017

CDRH Launches Expedited Access Pathway, Extends To De Novos

Apr 08 2015

House Set To Vote On Cures Nov. 30; Latest Version Includes 510(k)s In Breakthrough Pathway

Nov 28 2016

Additional Topics

United States Regulation Innovation Medical Device In Vitro Diagnostics

More from Regulation

More from Policy & Regulation

About Us

Meet the TeamOpens in new window
RSS FeedOpens in new window

Contact Us

Customer Service
SubscribeOpens in new window
AdvertisingOpens in new window
Feedback

Terms and ConditionsOpens in new window

Privacy PolicyOpens in new window