Federal (United States) · Regulations
Subpart E — Generally Recognized as Safe (GRAS) Notice
16 sections
16 sections
- 21 C.F.R. § 570.203Definitions.
- 21 C.F.R. § 570.205Opportunity to submit a GRAS notice.
- 21 C.F.R. § 570.210How to send your GRAS notice to FDA.
- 21 C.F.R. § 570.215Incorporation into a GRAS notice.
- 21 C.F.R. § 570.220General requirements applicable to a GRAS notice.
- 21 C.F.R. § 570.225Part 1 of a GRAS notice: Signed statements and certification.
- 21 C.F.R. § 570.230Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
- 21 C.F.R. § 570.235Part 3 of a GRAS notice: Target animal and human exposures.
- 21 C.F.R. § 570.240Part 4 of a GRAS notice: Self-limiting levels of use.
- 21 C.F.R. § 570.245Part 5 of a GRAS notice: Experience based on common use in food before 1958.
- 21 C.F.R. § 570.250Part 6 of a GRAS notice: Narrative.
- 21 C.F.R. § 570.255Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
- 21 C.F.R. § 570.260Steps you may take before FDA responds to your GRAS notice.
- 21 C.F.R. § 570.265What FDA will do with a GRAS notice.
- 21 C.F.R. § 570.275Public disclosure of a GRAS notice.
- 21 C.F.R. § 570.280Submission of a supplement.