Try our Advanced Search for more refined results

Abbott's Humira Letter Needed FDA's Green Light, Jury Told

By Megan Stride (April 25, 2013, 7:20 PM EDT) -- At a trial over claims that AbbVie Inc. and Abbott Laboratories failed to warn about Humira's risks, an AbbVie regulatory director testified Thursday that Abbott needed regulatory approval before it could send its May 2010 letter to doctors about the arthritis drug's link to undetected infections....

Law360 is on it, so you are, too.

A Law360 subscription puts you at the center of fast-moving legal issues, trends and developments so you can act with speed and confidence. Over 200 articles are published daily across more than 60 topics, industries, practice areas and jurisdictions.


A Law360 subscription includes features such as

  • Daily newsletters
  • Expert analysis
  • Mobile app
  • Advanced search
  • Judge information
  • Real-time alerts
  • 450K+ searchable archived articles

And more!

Experience Law360 today with a free 7-day trial.

Start Free Trial

Already a subscriber? Click here to login

Related Sections

Law Firms

Companies

Government Agencies

Hello! I'm Law360's automated support bot.

How can I help you today?

For example, you can type:
  • I forgot my password
  • I took a free trial but didn't get a verification email
  • How do I sign up for a newsletter?
Ask a question!