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2020-02-13
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Pre-Submission Consultation Process for Animal Food Additive Petitions or Generally Recognized as Safe Notices; Draft Guidance for Industry; Availability
Notices
D09002ee1be32168f
D09002ee1be32177d
United States
Department of Health and Human Services
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United States Government Agency or Subagency
United States
Food and Drug Administration
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United States Government Agency or Subagency
The Food and Drug Administration (FDA, we, or Agency) is announcing the availability of a draft guidance for industry (GFI) #262 entitled ``Pre-Submission Consultation Process for Animal Food Additive Petitions or Generally Recognized as Safe (GRAS) Notices.'' This draft guidance document, when finalized, will help industry submit information for effective and efficient consultations with FDA regarding investigational animal food substances.
85 FR 8297
https://www.govinfo.gov/app/details/FR-2020-02-13/2020-02867
2020-02867
fr13fe20-65
4164-01-P
Docket No. FDA-2020-D-0064
https://www.govinfo.gov/app/details/FR-2020-02-13/2020-02867
https://www.govinfo.gov/content/pkg/FR-2020-02-13/html/2020-02867.htm
https://www.govinfo.gov/content/pkg/FR-2020-02-13/pdf/2020-02867.pdf
2 p.
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85 FR 8297
Pre-Submission Consultation Process for Animal Food Additive Petitions or Generally Recognized as Safe Notices; Draft Guidance for Industry; Availability; Federal Register Vol. 85, Issue
NOTICE
2020-02867
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
2020-04-13
Docket No. FDA-2020-D-0064
4164-01-P
2020-02867
Notice of availability.
The Food and Drug Administration (FDA, we, or Agency) is announcing the availability of a draft guidance for industry (GFI) #262 entitled ``Pre-Submission Consultation Process for Animal Food Additive Petitions or Generally Recognized as Safe (GRAS) Notices.'' This draft guidance document, when finalized, will help industry submit information for effective and efficient consultations with FDA regarding investigational animal food substances.
Submit either electronic or written comments on the draft guidance by April 13, 2020 to ensure that the Agency considers your comment on this draft guidance before it begins work on the final version of the guidance.
Ciro Ruiz-Feria, Center for Veterinary Medicine (HFV-229), Food and Drug Administration, 7519 Standish Pl., Rockville, MD 20855, 240-402-6282, Ciro.Ruiz-Feria@fda.hhs.gov.
Guidance:
Pre-Submission Consultation Process for Animal Food Additive Petitions or Generally Recognized as Safe Notices,
Ciro.Ruiz-Feria@fda.hhs.gov
https://www.fda.gov/AnimalVeterinary/GuidanceComplianceEnforcement/GuidanceforIndustry/default.htm
https://www.govinfo.gov/content/pkg/FR-2015-09-18/pdf/2015-23389.pdf
https://www.regulations.gov
Federal Register
Vol. 85, no. 30
Office of the Federal Register, National Archives and Records Administration
2020-02-13
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daily
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253 p.
Table of Contents:
AE 2.7:
GS 4.107:
AE 2.106:
KF70.A2
https://www.govinfo.gov/app/details/FR-2020-02-13
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https://www.govinfo.gov/app/details/FR-2020-02-13
https://www.govinfo.gov/content/pkg/FR-2020-02-13/pdf/FR-2020-02-13.pdf
https://www.govinfo.gov/content/pkg/FR-2020-02-13/xml/FR-2020-02-13.xml
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2020-02-13
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FR-2020-02-13
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FR-2020-02-13
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