The U.S. Food and Drug Administration
FDA Issues CBD Warning Letters
The U.S. Food and Drug Administration (FDA) recently issued warning letters to 15 companies for, according the agency, illegally selling products containing cannabidiol (CBD) in ways that violate the Federal Food, Drug, and Cosmetic Act (FD&C Act). The FDA also published a revised Consumer Update detailing safety concerns about CBD products more broadly. The agency stated, based ...
CBD Usage Drops Sharply When Consumers Learn FDA Has No Safety Standards
In a warning sign for the burgeoning hemp and CBD industry, a new poll shows that 44 percent of Americans are less likely to use CBD products after learning that the U.S. Food and Drug Administration (FDA) has no standards in place to protect consumers, including 30 percent who say they would be far less ...
Homeopathic Association Works with FDA to Educate Manufacturers
The American Association of Homeopathic Pharmacists’ (AAHP) latest educational webinar illustrates the homeopathic industry fostering a relationship with the U.S. Food and Drug Administration (FDA) to ensure the highest quality of safe medicines to retailers, consumers and health practitioners across the U.S. Per the request of AAHP, the agency provided staff to present updates on its Compliance Policy for homeopathic products directly to ...
FDA Recognizes Canada as Having a Comparable Food Safety System to the U.S.
The U.S. Food and Drug Administration (FDA) signed an arrangement with the Canadian Food Inspection Agency (CFIA) and the Department of Health Canada (Health Canada) recognizing each other’s food safety systems as comparable to each other. The arrangement was signed at a meeting of the FDA-CFIA Health Canada Joint Committee on Food Safety. This is the second ...
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