21 CFR Subpart E
Generally Recognized as Safe (GRAS) Notice
June 25, 2020
§
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
§
570.265
What FDA will do with a GRAS notice
§
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
§
570.275
Public disclosure of a GRAS notice
§
570.280
Submission of a supplement
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