Posted May 7, 2015
Industry critics are calling for harsher regulations from the Food and Drug Administration (FDA) on homeopathic products that would affect consumer access to a wide range of homeopathic products, including calling for their removal from the marketplace. If the FDA begins to require additional premarket authorization processes, it will become overwhelming and will likely create a three-year backlog that will interfere with the innovation of new homeopathic remedies and block consumer access to products. Read more and TAKE ACTION NOW to tell the FDA to protect consumer access to homeopathic products.