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1. www.ecfr.gov › current › title-21eCFR :: 21 CFR Part 117 -- Current Good Manufacturing ...

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   The Code of Federal Regulations (CFR) is the official legal print publication containing the codification of the general and permanent rules published in the Federal Register by the departments and agencies of the Federal Government. The Electronic Code of Federal Regulations (eCFR) is a continuously updated online version of the CFR.

   • Applicability of Subparts C, D, and G of This Part to a Facility Solely Engaged in The Storage of Unexposed Packaged Food

     The Code of Federal Regulations (CFR) is the official legal...

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     The Code of Federal Regulations (CFR) is the official legal...

2. www.accessdata.fda.gov › CFRSearchCFR - Code of Federal Regulations Title 21 - Food and Drug ...

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   Dec 22, 2023 · The information on this page is current as of Dec 22, 2023. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). § 117.1 - Applicability and status. § 117.3 - Definitions. § 117.4 - Qualifications of individuals who manufacture, process, pack, or hold food. § 117.5 - Exemptions.

3. People also ask

   What are cGMPs in 21 CFR Part 117?

   • In addition to the CGMPs in Part 117, FDA has issued CGMPs specific to certain types of food. In 21 CFR Part 117 , FDA established a CGMP regulation as part of the “ Current Good Manufacturing Practice, Hazard Analysis, and Risk Based Preventive Controls for Human Food ” rule.

   CGMPs for Food and Dietary Supplements

   www.fda.gov/food/guidance-regulation-food-and-dietary-supplements/current-good-manufacturing-practices-cgmps-food-and-dietary-supplements

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   What is the latest version of CFR Title 21?

   • The information on this page is current as of Dec 22, 2023. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). Sec. 117.10 Personnel. (a) Disease control.

   CFR - Code of Federal Regulations Title 21 - Food and Drug Administrat…

   www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?CFRPart=117&showFR=1&subpartNode=21:2.0.1.1.16.2

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   When did cGMPs become a part 117?

   • In September 2015, the agency modernized the CGMPs and established them in new Part 117 ( 21 CFR Part 117 ), along with new requirements for hazard analysis and risk-based preventive controls which where were issued as part of the implementation of the FDA Food Safety Modernization Act (FSMA).

   CGMPs for Food and Dietary Supplements

   www.fda.gov/food/guidance-regulation-food-and-dietary-supplements/current-good-manufacturing-practices-cgmps-food-and-dietary-supplements

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   What does 117 201 & 117.251 mean?

   • § 117.201 - Modified requirements that apply to a qualified facility. § 117.206 - Modified requirements that apply to a facility solely engaged in the storage of unexposed packaged food. § 117.251 - Circumstances that may lead FDA to withdraw a qualified facility exemption.

   CFR - Code of Federal Regulations Title 21 - Food and Drug Administrat…

   www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfCFR/CFRSearch.cfm?CFRPart=117

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4. www.accessdata.fda.gov › scripts › cdrhCFR - Code of Federal Regulations Title 21 - Food and Drug ...

   www.accessdata.fda.gov › scripts › cdrh

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   Dec 22, 2023 · The information on this page is current as of Dec 22, 2023. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). Sec. 117.10 Personnel. (a) Disease control. Any person who, by medical examination or supervisory observation, is shown to have, or appears to have, an illness, open lesion ...

5. www.accessdata.fda.gov › scripts › cdrhCFR - Code of Federal Regulations Title 21 - Food and Drug ...

   www.accessdata.fda.gov › scripts › cdrh

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   Dec 22, 2023 · The information on this page is current as of Dec 22, 2023. For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). Sec. 117.201 Modified requirements that apply to a qualified facility. (a) Attestations to be submitted. A qualified facility must submit the following attestations to FDA:

6. www.law.cornell.edu › cfr › text21 CFR Part 117 - LII / Legal Information Institute

   www.law.cornell.edu › cfr › text

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   Electronic Code of Federal Regulations (e-CFR) Title 21—Food and Drugs; ... 21 CFR Part 117 - PART 117—CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND ...

7. ecfr.io › Title-21 › Part-11721 CFR 117 - eCFR - Electronic Code of Federal Regulations e-CFR

   ecfr.io › Title-21 › Part-117

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   Sep 17, 2015 · 117.7 Applicability of subparts C, D, and G of this part to a facility solely engaged in the storage of unexposed packaged food. 21:2.0.1.1.16.1.1.6 SECTION 117.8

8. www.fda.gov › food › guidance-regulation-food-andCurrent Good Manufacturing Practices (CGMPs) for Food and ...

   www.fda.gov › food › guidance-regulation-food-and

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   In 1969, FDA established CGMPs in the Code of Federal Regulations (CFR) (21 CFR Part 110). ... CGMPs in CFR 21 Part 117. In 21 CFR Part 117, FDA established a CGMP regulation as part of the ...