FDA Road To Decision On Expanding CBD Uses Starts With Weighing Impact On Existing And Future Use As Drug

At public hearing, FDA officials starting with acting Commissioner Sharpless emphasized CBD is approved only as a drug and deciding on allowing its use in any other type of FDA-regulated product will be done with potential impact on drug development foremost in agency's thinking. Also apparent from questions 12-member panel of FDA officials asked was a potential regulatory pathway for clearing hemp and CBD as dietary ingredients will require resolving concerns about the substances' dose or concentration levels and establishing ingredient identity standards.

CBD Molecule

US Food and Drug Administration officials are making clear that their consideration of cannabidiol's use as a dietary ingredient will prioritize weighing the potential impact of slowing or interrupting the development of drugs using cannabis-derived substances.

At a May 31 public hearing, officials starting with acting Commissioner Norman "Ned" Sharpless emphasized that CBD is approved only as a drug ingredient and deciding whether to allow it use in any other type of FDA-regulated product will be

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on HBW Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Regulation

More from Policy & Regulation