FDA to Evaluate Homeopathy Regulatory Framework

SEND YOUR TESTIMONY ABOUT HOMEOPATHY TO THE FDA

First published 24th March. Updated 26th March 2015.

(Reuters) - The U.S. Food and Drug Administration said it would hold a public hearing seeking information and comment on the use of products labeled 'homeopathic', as well as the agency's regulatory framework for such products.

The hearing, scheduled for April 20-21, will discuss prescription drugs, biological products, and over-the-counter drugs labeled homeopathic, a market that has expanded to become a multimillion dollar industry in the United States.

The agency is set to evaluate its regulatory framework for homeopathic products after a quarter century. (1.usa.gov/1Hxwup3)

http://www.reuters.com/article/2015/03/26/us-fda-homeopathy-idUSKBN0MM2PD20150326

Should FDA Make Changes to the Way it Regulates Homeopathic Products? Agency Wants to Know?

24th March 2015

 

by Alexander Gaffney, RAC
 
 
 
 
FDA to Assess Homeopathy Business