News & Analysis as of

Food and Drug Administration (FDA) › Defect

Gardner Law

Do you know when to report a medical device complaint?

Gardner Law on

Whether you manufacture a Class I elastic bandage or a Class III deep-brain stimulation device, understanding when to report a medical device complaint is critical and is also required for all FDA regulated medical devices....more

Searcy Denney Scarola Barnhart & Shipley

Closing the Loop-Holes in Generic Drug Warnings

Searcy Denney Scarola Barnhart & Shipley on

The Food and Drug Administration is considering some very important changes to its internal rules that would help to eliminate a loophole in accountability for defective drugs. Under current law, only the brand name...more

2 Results
 / 
View per page
Page: of 1

"My best business intelligence, in one easy email…"

Your first step to building a free, personalized, morning email brief covering pertinent authors and topics on JD Supra:
Sign up Log in
*By using the service, you signify your acceptance of JD Supra's Privacy Policy.
- hide
- hide