Dietary supplements Compliance

Dietary supplements Compliance & Quality Solutions

Dietary supplements are taken to improve overall health and to meet the daily requirement of essential nutrients. They come in many forms including tablets, capsules, soft gels, gel caps, powders, bards, gummies, and liquids.
Common dietary supplements include vitamins, minerals, botanical products, amino acids, and live microbial. (e.g., probiotics)
As per grand view research, the dietary supplements market size was valued at approximately 164 billion USD in 2022 and is expected to grow annually at a rate of 9%. With the increasing awareness around consumer health, dietary supplements are becoming routine products for daily life functioning.

The FDA does not approve any dietary supplements. As a manufacturer, importer, or distributor the company is responsible for the safety, efficacy, and labeling of products meeting applicable FDA and DHSEA regulations. It is critical to ensure that market claims are not made which may classify the dietary supplement as a drug.
FDA periodically inspects dietary supplement manufacturing facilities, review new dietary ingredient notifications and other regulatory submissions for dietary supplements, investigates complaints, monitors the dietary supplement marketplace, examines dietary supplements and ingredients for import, and reviews adverse even reports.
The Federal Trade Commission (FTC) regulates advertising, including infomercials, for dietary supplements.
Both FDA and FTC have the authority to take enforcement actions against dietary supplements and firms if they identify violations which include warning letters, fines, recalls, or stop sales.