FDA Oversight Of Lab-Developed Tests Is Likely To Lessen

Law360, New York (March 1, 2017, 1:05 PM EST) -- On Jan. 13, 2017, the U.S. Food and Drug Administration issued a discussion paper on laboratory developed tests (LDTs).[1] The discussion paper follows FDA's late 2016 announcement[2] that, contrary to the agency's earlier reports, it would not issue a final guidance on its proposed oversight of LDTs to allow "for further public discussion on an appropriate oversight approach, and to give our congressional authorizing committees the opportunity to develop a legislative solution."[3]...

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

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!