FDA Warning Letters
Homeopathic Companies Suspend Marketing of Eye Care Products After Receiving FDA Warning Letters
In September, the U.S. Food and Drug Administration (FDA) sent warning letters to eight companies, including six homeopathic product manufacturers, for “manufacturing or marketing ophthalmic drug products in violation of federal law.” According to FDA, the letters are part of an ongoing effort to crack down on ophthalmic products that are illegally marketed to treat ...
AHPA President Provides Supplement Regulation Compliance Strategies
American Herbal Products Association (AHPA) President Michael McGuffin provided an overview of supplement regulations and compliance strategies at the Best Practices in QC, GMP for Dietary Supplements and Nutraceuticals Effective Compliance Seminar in Salt Lake City. McGuffin’s presentation covered a wide-range of supplement regulatory issues from current good manufacturing practice (cGMP) requirements and Food and ...
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