Subpart E. Subpart E—Generally Recognized as Safe (GRAS) Notice
- § 170.203 - Definitions.
- § 170.205 - Opportunity to submit a GRAS notice.
- § 170.210 - How to send your GRAS notice to FDA.
- § 170.215 - Incorporation into a GRAS notice.
- § 170.220 - General requirements applicable to a GRAS notice.
- § 170.225 - Part 1 of a GRAS notice: Signed statements and certification.
- § 170.230 - Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
- § 170.235 - Part 3 of a GRAS notice: Dietary exposure.
- § 170.240 - Part 4 of a GRAS notice: Self-limiting levels of use.
- § 170.245 - Part 5 of a GRAS notice: Experience based on common use in food before 1958.
- § 170.250 - Part 6 of a GRAS notice: Narrative.
- § 170.255 - Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
- § 170.260 - Steps you may take before FDA responds to your GRAS notice.
- § 170.265 - What FDA will do with a GRAS notice.
- § 170.270 - Procedures 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.
- § 170.275 - Public disclosure of a GRAS notice.
- § 170.280 - Submission of a supplement.
- § 170.285 - Disposition of pending GRAS affirmation petitions.