US FDA/CFSAN - Implementation of FDA's Current Good Manufacturing Practices for Dietary Supplements
October 24, 2007
IFR
- If the petition is granted, § 111.75(a)(1)(i) would require the manufacturer to implement the system identified in the petition.
- scientific method developed by the manufacturer
- identity may include physical characteristics (such as crystal or powder), state of hydration, or part of the plant (roots or leaves). The term ''identity'' would include the manufacturer's specification (s) that would identify the attributes a supplier must meet. demonstrating that less than 100 percent identity testing did not materially diminish assurance that the dietary ingredient is the correct dietary ingredient.