21 CFR Part 570 - Subpart E - Generally Recognized as Safe (GRAS) Notice
- § 570.203 Definitions.
- § 570.205 Opportunity to submit a GRAS notice.
- § 570.210 How to send your GRAS notice to FDA.
- § 570.215 Incorporation into a GRAS notice.
- § 570.220 General requirements applicable to a GRAS notice.
- § 570.225 Part 1 of a GRAS notice: Signed statements and certification.
- § 570.230 Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
- § 570.235 Part 3 of a GRAS notice: Target animal and human exposures.
- § 570.240 Part 4 of a GRAS notice: Self-limiting levels of use.
- § 570.245 Part 5 of a GRAS notice: Experience based on common use in food before 1958.
- § 570.250 Part 6 of a GRAS notice: Narrative.
- § 570.255 Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
- § 570.260 Steps you may take before FDA responds to your GRAS notice.
- § 570.265 What FDA will do with a GRAS notice.
- § 570.275 Public disclosure of a GRAS notice.
- § 570.280 Submission of a supplement.
Source:
81 FR 55052, Aug. 17, 2016, unless otherwise noted.