Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food For Animals

 
Docket ID: FDA-2011-N-0922
Agency: Food and Drug Administration (FDA)
Parent Agency: Department of Health and Human Services (HHS)
Summary:

This rule establishes requirements for good manufacturing practice, and requires that certain facilities establish and implement hazard analysis and risk-based preventive controls for animal food, including ingredients and mixed animal feed. This action is intended to provide greater assurance that food for all animals, including pets, is safe.

RIN: 0910-AG10
Impacts and Effects: International
CFR Citation: 21 CFR 507
Priority: Economically Significant
UA and Regulatory Plan Information open glossary dialog  
Publication Period: Fall 2015
Agenda Stage of Rulemaking: Completed Action
Major Rule: Yes
Legal Authorities: 21 U.S.C. 321, 21 U.S.C. 331, 21 U.S.C. 342, 21 U.S.C. 350c, 21 U.S.C. 350d note, 21 U.S.C. 350g, 21 U.S.C. 350g note, 21 U.S.C. 371, 21 U.S.C. 374, 42 U.S.C. 264, 42 U.S.C. 243, 42 U.S.C. 271, ...
Government Levels Affected: State
Federalism Implications: Yes
Unfunded Mandates: Private Sector
Requires Regulatory Flexibility Analysis: Business
Small Entities Affected: No
International Impacts: Yes
Included in Regulatory Plan: No
Legal Deadline
ActionSourceDescriptionDate
JudicialOther08/30/2015
Timetable
ActionDateFR Citation
NPRM10/29/201378 FR 64736
NPRM Comment Period Extension02/03/201479 FR 6111
NPRM Comment Period End02/26/2014
NPRM Comment Period Extension End03/31/2014
Supplemental NPRM09/29/201479 FR 58475
Supplemental NPRM Comment Period End12/15/2014
Final Rule09/17/201580 FR 56169
Final Rule Effective11/16/2015
Docket Details open glossary dialog  
Related RINs: None
Related Dockets: None
Short Title: Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Food For Animals
Keyword(s): 0910-AG10, of, of20114, food for animals, hazard analysis, 2012-62, 0910-0789, 2015-1037
Type: Rulemaking
Docket Status: OPEN
Center: CVM
Docket Item Code: N
 

Primary Documents

View All  (17)
Comment Period Closed
Dec 15, 2014 11:59 PM ET
Proposed Rule
Posted: 09/29/2014
ID: FDA-2011-N-0922-0269
Comment Period Closed
Mar 31, 2014 11:59 PM ET
Proposed Rule
Posted: 02/03/2014
ID: FDA-2011-N-0922-0019
Comment Period Closed
Feb 26, 2014 11:59 PM ET
Proposed Rule
Posted: 10/29/2013
ID: FDA-2011-N-0922-0002
Comment Period Closed
Rule
Posted: 01/22/2016
ID: FDA-2011-N-0922-0553
Comment Period Closed
Notice
Posted: 11/13/2015
ID: FDA-2011-N-0922-0552

Supporting Documents

View All  (156)
Comments Not Accepted
Supporting & Related Material
Posted: 09/22/2015
ID: FDA-2011-N-0922-0551
Comments Not Accepted
Supporting & Related Material
Posted: 09/17/2015
ID: FDA-2011-N-0922-0535
Comments Not Accepted
Supporting & Related Material
Posted: 09/17/2015
ID: FDA-2011-N-0922-0536

Comments

View All  (389)

2,269
Comments Received*
Regulatory Timeline
Pre Rule
Current Stage
Proposed Rule
Current Stage
Final Rule
Current Stage
Completed
Current Stage
Agency Contact
Jeanette (Jenny) B. Murphy
Consumer Safety Officer
FDA/HHS
Center for Veterinary Medicine, Room 2671 (MPN-4, HFV-200), 7519 Standish Place
Rockville, MD 20855
*This count refers to the total comment/submissions received on this docket, as of 11:59 PM yesterday. Note: Agencies review all submissions, however some agencies may choose to redact, or withhold, certain submissions (or portions thereof) such as those containing private or proprietary information, inappropriate language, or duplicate/near duplicate examples of a mass-mail campaign. This can result in discrepancies between this count and those displayed when conducting searches on the Public Submission document type. For specific information about an agency’s public submission policy, refer to its website or the Federal Register document.