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HHS/FDA | RIN: 0910-AG36 | Publication ID: Fall 2010 |
Title: Modernization of the Current Food Good Manufacturing Practices Regulation | |
Abstract: The Food and Drug Administration (FDA) is proposing to amend its current good manufacturing practices (CGMP) regulations (21 CFR part 110) for manufacturing, packing, or holding human food. This proposed rule would require food facilities to address issues such as environmental pathogens, food allergens, mandatory employee training, and sanitation of food contact surfaces. The proposed rule also would require food facilities to develop and implement preventive control systems. FDA is taking this action to better address changes that have occurred in the food industry and protect public health. | |
Agency: Department of Health and Human Services(HHS) | Priority: Economically Significant |
RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Long-Term Actions |
Major: Yes | Unfunded Mandates: No |
CFR Citation: 21 CFR 110 | |
Legal Authority: 21 USC 342 21 USC 371 42 USC 264 |
Legal Deadline:
None |
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Timetable:
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Regulatory Flexibility Analysis Required: Yes | Government Levels Affected: None |
Small Entities Affected: Businesses | Federalism: Undetermined |
Included in the Regulatory Plan: No | |
International Impacts: This regulatory action will be likely to have international trade and investment effects, or otherwise be of international interest. | |
RIN Data Printed in the FR: Yes | |
Agency Contact: Paul South Department of Health and Human Services Food and Drug Administration Center for Food Safety and Applied Nutrition (HFS-317), Office of Food Safety, 5100 Paint Branch Parkway, College Park, MD 20740 Phone:301 436-1640 Email: paul.south@fda.hhs.gov |