Dietary Supplement Testing Fda

This is not unexpected.
Dietary supplement testing fda. The only way to ensure that a dietary supplement meets the. The fda wants to make sure dietary supplement makers are using safe and honest marketing for example. These include monitoring mandatory reporting of serious adverse events by dietary supplement firms.
Fda is applying greater attention to and enforcement of dietary supplement regulations than ever before. The fda oversees the manufacturing testing and sales practices of many industries including the dietary supplement industry. To contact the office of dietary supplement programs email.
Office of dietary supplement programs hfs 810 food and drug administration 5001 campus dr college park md 20740. Import alert 54 17 on ayurvedic dietary supplements. Although dietary supplements do not receive the same regulation as otc or pharmaceutical drugs their testing standards are becoming more strict.
Any testing method must be scientifically valid and qualified by the lab performing them. Npa believes the fda was responsive to the many industry comments submitted in response to the proposed fda gmps in 2003 objecting to the heavy emphasis on finished product testing especially the requirements for testing every batch of finished dietary supplements for identity quality strength purity and composition the understanding being. Fda has the authority to take enforcement action when foods including dietary supplements are found through routine or targeted testing to.
Guidance and regulatory information on food and dietary supplements. In fact the fda states that dietary supplements are regulated and these regulations apply to both manufacturers and distributors. Once a dietary supplement is on the market fda has certain safety monitoring responsibilities.
Labs must be transparent in disclosure of the required work as well open to a formal audit.