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HHS/FDA RIN: 0910-AH77 Publication ID: Spring 2019 
Title: Streamlining Provisions For Disclosure to Commercial Customers and Receipt of Written Assurance From Commercial Customers in the Current Good Manufacturing Practice and Preventive Control Human Food 
Abstract:

This proposed rule would remove certain requirements that currently apply when a manufacturer/processor of human food has identified a hazard that requires a preventive control, but does not control that hazard. Although that manufacturer/processor would still be required to provide documentation that the food has not been processed to control the identified hazard, that manufacturer/processor would no longer be required to obtain written assurance from the commercial customer that the identified hazard will be controlled. 

 
Agency: Department of Health and Human Services(HHS)  Priority: Other Significant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Proposed Rule Stage 
Major: Undetermined  Unfunded Mandates: Undetermined 
EO 13771 Designation: Deregulatory 
CFR Citation: Not Yet Determined     (To search for a specific CFR, visit the Code of Federal Regulations.)
Legal Authority: Not Yet Determined   
Legal Deadline:  None
Timetable:
Action Date FR Cite
NPRM  05/00/2019 
Regulatory Flexibility Analysis Required: Undetermined  Government Levels Affected: Undetermined 
Federalism: Undetermined 
Included in the Regulatory Plan: No 
RIN Data Printed in the FR: No 
Agency Contact:
Jan Carlson
Special Assistant
Department of Health and Human Services
Food and Drug Administration
5001 Campus Drive, Room 4B009,
College Park, MD 20740
Phone:240 402-1788
Email: jan.carlson@fda.hhs.gov