Generics BulletinHBW InsightIn VivoMedtech InsightPink SheetScrip

Generics Bulletin

Medtech Insight

Industry Says MDR Draft Guidance Would Lead To Redundant Reporting

Oct 28 2013

Related Content

FDA’s Quest For More MDR Exemption Requests Leaves Device Industry Jittery

Aug 14 2013

FDA On The Lookout For Potential Recalls Masked As Service Requests

Mar 03 2008

Draft Guidance Tackles Common Errors In Adverse Event Reporting

Jul 08 2013

Additional Topics

Regulation Medical Device

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