Generics BulletinHBW InsightIn VivoMedtech InsightPink SheetScrip

Generics Bulletin

Medtech Insight

Draft Guidance Offers Clarity On 510(k) Need for Software Modifications

Aug 09 2016

Related Content

FDA Calls For Full Risk Reviews For Device Changes In 510(k) Modifications Draft

Aug 05 2016

Additional Topics

United States Regulation Medical Device

More from Regulation

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