21 CFR Subpart E
Generally Recognized as Safe (GRAS) Notice
June 25, 2020
§
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
§
170.203
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
§
170.250
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