BACKGROUND AND OBJECTIVES: Electronic personal health records (PHRs) allow patients access to their medical records, self-management tools, and new avenues of communication with their health care providers.
FDA issues guidance on antioxidants. The US Food and Drug Administration (FDA) has published guidance to help small companies comply with the labeling of antioxidant products and high potency products. The Small Entity Compliance Guide sets out the agencyâs position âin plain languageâ regarding the use of the nutrient content claims on dietary supplement products.
The FDA (Food and Drug Administration) is a government agency responsible for upholding and protecting the safety and health of the United States' general public.he FDA promotes these goals through the implementation of standards regarding food, medications, medical devices, cosmetics, dietary supplements and tobacco. If a manufacturer, seller or distributor fails to comply with FDA regulations they will be liable for an assortment of felony charges.