Generics BulletinHBW InsightIn VivoMedtech InsightPink SheetScrip

Generics Bulletin

Medtech Insight

FDA Releases Guidance Documents On PMA, 510(k) Review Times And Goals

Oct 22 2012

Related Content

FDA Embraces Total-Time Pre-Market Review Goals, With Shared Accountability

Oct 10 2011

Device Industry Expects Quicker Path To Market In Exchange For Doubling Of User Fees

Feb 06 2012

Final FDA Bill: Device Provisions

Jun 25 2012

Additional Topics

Legislation Regulation Medical Device

More from Legislation

More from Policy & Regulation

Twitter feed RSS feed RSS feed

About UsOpens in new window
Meet the TeamOpens in new window
RSS FeedOpens in new window

Contact Us
Customer Service
Subscribe
AdvertisingOpens in new window
Feedback

Terms and ConditionsOpens in new window

Privacy PolicyOpens in new window