Federal (United States) · Regulations
Subpart E — Generally Recognized as Safe (GRAS) Notice
18 sections
18 sections
- 21 C.F.R. § 170.203Definitions.
- 21 C.F.R. § 170.205Opportunity to submit a GRAS notice.
- 21 C.F.R. § 170.210How to send your GRAS notice to FDA.
- 21 C.F.R. § 170.215Incorporation into a GRAS notice.
- 21 C.F.R. § 170.220General requirements applicable to a GRAS notice.
- 21 C.F.R. § 170.225Part 1 of a GRAS notice: Signed statements and certification.
- 21 C.F.R. § 170.230Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
- 21 C.F.R. § 170.235Part 3 of a GRAS notice: Dietary exposure.
- 21 C.F.R. § 170.240Part 4 of a GRAS notice: Self-limiting levels of use.
- 21 C.F.R. § 170.245Part 5 of a GRAS notice: Experience based on common use in food before 1958.
- 21 C.F.R. § 170.250Part 6 of a GRAS notice: Narrative.
- 21 C.F.R. § 170.255Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
- 21 C.F.R. § 170.260Steps you may take before FDA responds to your GRAS notice.
- 21 C.F.R. § 170.265What FDA will do with a GRAS notice.
- 21 C.F.R. § 170.270Procedures that apply when the intended conditions of use of a notified substance include use in a product or products subject to regulation by the Food Safety and Inspection Service (FSIS) of the United States Department of Agriculture.
- 21 C.F.R. § 170.275Public disclosure of a GRAS notice.
- 21 C.F.R. § 170.280Submission of a supplement.
- 21 C.F.R. § 170.285Disposition of pending GRAS affirmation petitions.