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Generally Recognized as Safe (GRAS) Notice
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Animal Drugs, Feeds, and Related Products
Food Additives
Generally Recognized as Safe (GRAS) Notice
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Section
570.203
Definitions.
Section
570.205
Opportunity to submit a GRAS notice.
Section
570.210
How to send your GRAS notice to FDA.
Section
570.215
Incorporation into a GRAS notice.
Section
570.220
General requirements applicable to a GRAS notice.
Section
570.225
Part 1 of a GRAS notice: Signed statements and certification.
Section
570.230
Part 2 of a GRAS notice: Identity, method of manufacture, specifications, and physical or technical effect.
Section
570.235
Part 3 of a GRAS notice: Target animal and human exposures.
Section
570.240
Part 4 of a GRAS notice: Self-limiting levels of use.
Section
570.245
Part 5 of a GRAS notice: Experience based on common use in food before 1958.
Section
570.250
Part 6 of a GRAS notice: Narrative.
Section
570.255
Part 7 of a GRAS notice: List of supporting data and information in your GRAS notice.
Section
570.260
Steps you may take before FDA responds to your GRAS notice.
Section
570.265
What FDA will do with a GRAS notice.
Section
570.275
Public disclosure of a GRAS notice.
Section
570.280
Submission of a supplement.