{"description":"Documents matching 'compliance guide secg help small'","count":77,"total_pages":4,"next_page_url":"https://www.federalregister.gov/api/v1/documents?conditions%5Bterm%5D=compliance+guide+secg+help+small&format=json&page=2","results":[{"title":"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption: What You Need To Know About the Food and Drug Administration Regulation; Small Entity Compliance Guide; Availability","type":"Rule","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is announcing the availability of a guidance for industry entitled \"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption: What You Need to Know About the FDA Regulation: Small Entity Compliance Guide.\" We are updating the small entity compliance guide (SECG) to help small entities comply with revised requirements related to agricultural water in the \"Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption\" regulation.","document_number":"2024-21840","html_url":"https://www.federalregister.gov/documents/2024/09/24/2024-21840/standards-for-the-growing-harvesting-packing-and-holding-of-produce-for-human-consumption-what-you","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-09-24/pdf/2024-21840.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-21840.pdf?1727095535","publication_date":"2024-09-24","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"Agency, or we) is announcing the availability of a guidance for industry entitled “Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption: What You Need to Know About the FDA Regulation: <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>.” We are updating the <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) to <span class=\"match\">help</span> <span class=\"match\">small</span> entities comply with revised requirements related to agricultural water in the “Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption” regulation. \n \n \n DATES: \n \n The announcement of the"},{"title":"Mammography Quality Standards Act and Regulation Amendments: Small Entity Compliance Guide; Guidance for Industry and Food and Drug Administration Staff; Availability","type":"Rule","abstract":"The Food and Drug Administration (FDA or the Agency) is announcing the availability of a guidance for industry entitled \"Mammography Quality Standards Act and Regulation Amendments: Small Entity Compliance Guide.\" The Mammography Quality Standards Act of 1992 (MQSA) final rule amended FDA's regulations to address, among other things, standards for accreditation bodies, certifying agencies, mammography equipment, quality assurance testing, and clinical image quality, as well as to require certain breast density information be provided by mammography facilities to patients and their healthcare providers. The small entity compliance guide (SECG) is intended to help small entities comply with the MQSA final rule.","document_number":"2024-19059","html_url":"https://www.federalregister.gov/documents/2024/08/26/2024-19059/mammography-quality-standards-act-and-regulation-amendments-small-entity-compliance-guide-guidance","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-08-26/pdf/2024-19059.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-19059.pdf?1724417123","publication_date":"2024-08-26","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"Act and Regulation Amendments: <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>.” The Mammography Quality Standards Act of 1992 (MQSA) final rule amended FDA's regulations to address, among other things, standards for accreditation bodies, certifying agencies, mammography equipment, quality assurance testing, and clinical image quality, as well as to require certain breast density information be provided by mammography facilities to patients and their healthcare providers. The <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) is intended to <span class=\"match\">help</span> <span class=\"match\">small</span> entities comply with the MQSA"},{"title":"Federal Acquisition Regulation; Federal Acquisition Circular 2025-03; Small Entity Compliance Guide","type":"Rule","abstract":"This document is issued under the joint authority of DoD, GSA, and NASA. This Small Entity Compliance Guide has been prepared in accordance with section 212 of the Small Business Regulatory Enforcement Fairness Act of 1996. It consists of a summary of the rules appearing in Federal Acquisition Circular (FAC) 2025-03, which amends the Federal Acquisition Regulation (FAR). Interested parties may obtain further information regarding these rules by referring to FAC 2025-03, which precedes this document.","document_number":"2024-31408","html_url":"https://www.federalregister.gov/documents/2025/01/03/2024-31408/federal-acquisition-regulation-federal-acquisition-circular-2025-03-small-entity-compliance-guide","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-01-03/pdf/2024-31408.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-31408.pdf?1735825512","publication_date":"2025-01-03","agencies":[{"raw_name":"DEPARTMENT OF DEFENSE","name":"Defense Department","id":103,"url":"https://www.federalregister.gov/agencies/defense-department","json_url":"https://www.federalregister.gov/api/v1/agencies/103","parent_id":null,"slug":"defense-department"},{"raw_name":"GENERAL SERVICES ADMINISTRATION","name":"General Services Administration","id":210,"url":"https://www.federalregister.gov/agencies/general-services-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/210","parent_id":null,"slug":"general-services-administration"},{"raw_name":"NATIONAL AERONAUTICS AND SPACE ADMINISTRATION","name":"National Aeronautics and Space Administration","id":301,"url":"https://www.federalregister.gov/agencies/national-aeronautics-and-space-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/301","parent_id":null,"slug":"national-aeronautics-and-space-administration"}],"excerpts":"ACTION: \n <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span> (<span class=\"match\">SECG</span>). \n \n \n SUMMARY: \n \n This document is issued under the joint authority of DoD, GSA, and NASA. This \n <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span> \n has been prepared in accordance with section 212 of the <span class=\"match\">Small</span> Business Regulatory Enforcement Fairness Act of 1996. It consists of a summary of the rules appearing in Federal Acquisition Circular (FAC) 2025-03, which amends the Federal Acquisition Regulation (FAR). Interested parties may obtain further information regarding these rules by referring to FAC 2025-03, which"},{"title":"Revocation of Uses of Partially Hydrogenated Oils in Foods: Guidance for Industry; Small Entity Compliance Guide; Availability","type":"Rule","abstract":"The Food and Drug Administration (FDA or we) is announcing the availability of a guidance for industry entitled \"Revocation of Uses of Partially Hydrogenated Oils in Foods: Guidance for Industry; Small Entity Compliance Guide.\" The small entity compliance guide (SECG) is intended to help small entities comply with our regulations after we revoked specific requirements pertaining to the use of partially hydrogenated oils in certain foods or as a direct or indirect food substance.","document_number":"2024-08955","html_url":"https://www.federalregister.gov/documents/2024/04/29/2024-08955/revocation-of-uses-of-partially-hydrogenated-oils-in-foods-guidance-for-industry-small-entity","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-04-29/pdf/2024-08955.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-08955.pdf?1714135520","publication_date":"2024-04-29","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"availability. \n \n \n SUMMARY: \n The Food and Drug Administration (FDA or we) is announcing the availability of a guidance for industry entitled “Revocation of Uses of Partially Hydrogenated Oils in Foods: Guidance for Industry; <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>.” The <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) is intended to <span class=\"match\">help</span> <span class=\"match\">small</span> entities comply with our regulations after we revoked specific requirements pertaining to the use of partially hydrogenated oils in certain foods or as a direct or indirect food substance. \n \n \n DATES: \n \n The announcement of"},{"title":"Laboratory Developed Tests: Small Entity Compliance Guide; Guidance for Laboratory Manufacturers and Food and Drug Administration Staff; Availability","type":"Notice","abstract":"The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance entitled \"Laboratory Developed Tests: Small Entity Compliance Guide.\" The laboratory developed tests (LDT) final rule amended FDA's regulations to make explicit that in vitro diagnostic products (IVDs) are devices under the Federal Food, Drug, and Cosmetic Act (FD&C Act) including when the manufacturer of the IVD is a laboratory. This small entity compliance guide (SECG) is intended to help small entities comply with applicable medical device regulations, consistent with the LDT final rule, including the phasing out of FDA's general enforcement discretion approach for LDTs so that IVDs manufactured by a laboratory will generally fall under the same enforcement approach as other IVDs.","document_number":"2024-13872","html_url":"https://www.federalregister.gov/documents/2024/06/25/2024-13872/laboratory-developed-tests-small-entity-compliance-guide-guidance-for-laboratory-manufacturers-and","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-06-25/pdf/2024-13872.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-13872.pdf?1719233120","publication_date":"2024-06-25","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"Agency) is announcing the availability of a final guidance entitled “Laboratory Developed Tests: <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>.” The laboratory developed tests (LDT) final rule amended FDA's regulations to make explicit that in vitro diagnostic products (IVDs) are devices under the Federal Food, Drug, and Cosmetic Act (FD&amp;C Act) including when the manufacturer of the IVD is a laboratory. This <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) is intended to <span class=\"match\">help</span> <span class=\"match\">small</span> entities comply with applicable medical device regulations, consistent with the LDT final rule"},{"title":"Federal Acquisition Regulation; Federal Acquisition Circular 2025-03; Introduction","type":"Rule","abstract":"This document summarizes the Federal Acquisition Regulation (FAR) rules agreed to by the Civilian Agency Acquisition Council and the Defense Acquisition Regulations Council (Councils) in this Federal Acquisition Circular (FAC) 2025-03. A companion document, the Small Entity Compliance Guide (SECG), follows this FAC.","document_number":"2024-31409","html_url":"https://www.federalregister.gov/documents/2025/01/03/2024-31409/federal-acquisition-regulation-federal-acquisition-circular-2025-03-introduction","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2025-01-03/pdf/2024-31409.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-31409.pdf?1735825512","publication_date":"2025-01-03","agencies":[{"raw_name":"DEPARTMENT OF DEFENSE","name":"Defense Department","id":103,"url":"https://www.federalregister.gov/agencies/defense-department","json_url":"https://www.federalregister.gov/api/v1/agencies/103","parent_id":null,"slug":"defense-department"},{"raw_name":"GENERAL SERVICES ADMINISTRATION","name":"General Services Administration","id":210,"url":"https://www.federalregister.gov/agencies/general-services-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/210","parent_id":null,"slug":"general-services-administration"},{"raw_name":"NATIONAL AERONAUTICS AND SPACE ADMINISTRATION","name":"National Aeronautics and Space Administration","id":301,"url":"https://www.federalregister.gov/agencies/national-aeronautics-and-space-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/301","parent_id":null,"slug":"national-aeronautics-and-space-administration"}],"excerpts":"to by the Civilian Agency Acquisition Council and the Defense Acquisition Regulations Council (Councils) in this Federal Acquisition Circular (FAC) 2025-03. A companion document, the \n <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span> \n (<span class=\"match\">SECG</span>), follows this FAC.\n \n \n \n DATES: \n For effective dates see the separate documents, which follow. \n \n \n ADDRESSES: \n \n The FAC, including the <span class=\"match\">SECG</span>, is available at \n https://www.regulations.gov. \n \n \n \n FOR FURTHER INFORMATION CONTACT: \n \n The analyst whose name appears in the table below in relation to the FAR case. For information"},{"title":"Direct-to-Consumer Prescription Drug Advertisements: Presentation of the Major Statement in a Clear, Conspicuous, and Neutral Manner in Advertisements in Television and Radio Format Final Rule: Questions and Answers; Guidance for Industry; Small Entity Compliance Guide; Availability","type":"Rule","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is announcing the availability of a guidance for industry entitled \"Direct-to-Consumer Prescription Drug Advertisements: Presentation of the Major Statement in a Clear, Conspicuous, and Neutral Manner in Advertisements in Television and Radio Format Final Rule: Questions and Answers.\" We are issuing this small entity compliance guide (SECG) in accordance with the Small Business Regulatory Enforcement Fairness Act to help small businesses understand and comply with the \"Direct-to- Consumer Prescription Drug Advertisements: Presentation of the Major Statement in a Clear, Conspicuous, and Neutral Manner in Advertisements in Television and Radio Format Final Rule\" (CCN Final Rule). The CCN Final Rule modifies FDA regulations to reflect the requirement in the Federal Food, Drug, and Cosmetic Act (FD&C Act) that human prescription drug advertisements presented directly to consumers (DTC) in television or radio format and stating the name of the drug and its conditions of use (DTC TV/radio ads) present the major statement relating to side effects and contraindications (major statement) in a clear, conspicuous, and neutral manner and establishes standards to help ensure this requirement is met. The term \"drugs\" in this guidance refers to prescription human drug and biological products.","document_number":"2023-28530","html_url":"https://www.federalregister.gov/documents/2023/12/27/2023-28530/direct-to-consumer-prescription-drug-advertisements-presentation-of-the-major-statement-in-a-clear","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-12-27/pdf/2023-28530.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-28530.pdf?1703598330","publication_date":"2023-12-27","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"Prescription Drug Advertisements: Presentation of the Major Statement in a Clear, Conspicuous, and Neutral Manner in Advertisements in Television and Radio Format Final Rule: Questions and Answers.” We are issuing this <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) in accordance with the <span class=\"match\">Small</span> Business Regulatory Enforcement Fairness Act to <span class=\"match\">help</span> <span class=\"match\">small</span> businesses understand and comply with the “Direct-to-Consumer Prescription Drug Advertisements: Presentation of the Major Statement in a Clear, Conspicuous, and Neutral Manner in Advertisements in Television and Radio"},{"title":"Requirements for Additional Traceability Records for Certain Foods: What You Need To Know About the Food and Drug Administration Regulation: Guidance for Industry; Small Entity Compliance Guide; Availability","type":"Rule","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is announcing the availability of a guidance for industry entitled \"Requirements for Additional Traceability Records for Certain Foods: What You Need to Know About the FDA Regulation: Guidance for Industry-- Small Entity Compliance Guide.\" The small entity compliance guide (SECG) is intended to help small entities comply with the final rule entitled \"Requirements for Additional Traceability Records for Certain Foods.\"","document_number":"2023-10666","html_url":"https://www.federalregister.gov/documents/2023/05/19/2023-10666/requirements-for-additional-traceability-records-for-certain-foods-what-you-need-to-know-about-the","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-05-19/pdf/2023-10666.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-10666.pdf?1684413927","publication_date":"2023-05-19","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":" the Agency, or we) is announcing the availability of a guidance for industry entitled “Requirements for Additional Traceability Records for Certain Foods: What You Need to Know About the FDA Regulation: Guidance for Industry—<span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>.” The <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) is intended to <span class=\"match\">help</span> <span class=\"match\">small</span> entities comply with the final rule entitled “Requirements for Additional Traceability Records for Certain Foods.” \n \n \n DATES: \n \n The announcement of the guidance is published in the \n Federal Register \n on May 19, 2023.\n \n"},{"title":"Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; New Animal Drugs for Minor Use and Minor Species","type":"Notice","abstract":"The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.","document_number":"2026-13005","html_url":"https://www.federalregister.gov/documents/2026/06/29/2026-13005/agency-information-collection-activities-submission-for-office-of-management-and-budget-review","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2026-06-29/pdf/2026-13005.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2026-13005.pdf?1782477909","publication_date":"2026-06-29","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"information. One comment was received. While the commenter supported the collection of information requirements, they raised concerns about the administrative and financial burden on <span class=\"match\">smaller</span> companies, recommending that FDA develop templates or guidance materials to ease the process for these companies.\n \n \n FDA appreciates the comment. FDA provides a <span class=\"match\">Small</span> Business <span class=\"match\">Guide</span> on the Agency's website at \n http://www.fda.gov/ForIndustry/SmallBusinessAssistance/default.htm. \n FDA has also published the following Guidance for Industry (GFI) documents to assist"},{"title":"Regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products: Small Entity Compliance Guide; Availability","type":"Rule","abstract":"The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a final guidance entitled \"Regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/ Ps): Small Entity Compliance Guide.\" The small entity compliance guide (SECG) is intended to help small entity establishments that manufacture HCT/Ps better understand the comprehensive regulatory framework for HCT/Ps set forth in the regulations and comply with certain HCT/P- related final rules. The SECG announced in this notice supersedes the SECG of the same title dated August 2007.","document_number":"2022-23573","html_url":"https://www.federalregister.gov/documents/2022/11/01/2022-23573/regulation-of-human-cells-tissues-and-cellular-and-tissue-based-products-small-entity-compliance","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2022-11-01/pdf/2022-23573.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2022-23573.pdf?1667220319","publication_date":"2022-11-01","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"guidance entitled “Regulation of Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/Ps): <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>.” The <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) is intended to <span class=\"match\">help</span> <span class=\"match\">small</span> entity establishments that manufacture HCT/Ps better understand the comprehensive regulatory framework for HCT/Ps set forth in the regulations and comply with certain HCT/P-related final rules. The <span class=\"match\">SECG</span> announced in this notice supersedes the <span class=\"match\">SECG</span> of the same title dated August 2007. \n \n \n DATES: \n \n The announcement of the guidance is published in"},{"title":"Laboratory Accreditation for Analyses of Foods; Small Entity Compliance Guide; Availability","type":"Rule","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is announcing the availability of a guidance for industry entitled \"Laboratory Accreditation for Analyses of Foods: What You Need to Know About the FDA Regulation: Guidance for Industry--Small Entity Compliance Guide.\" The small entity compliance guide (SECG) is intended to help small entities comply with the final rule entitled \"Laboratory Accreditation for Analyses of Foods.\"","document_number":"2022-22706","html_url":"https://www.federalregister.gov/documents/2022/10/20/2022-22706/laboratory-accreditation-for-analyses-of-foods-small-entity-compliance-guide-availability","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2022-10-20/pdf/2022-22706.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2022-22706.pdf?1666183520","publication_date":"2022-10-20","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"Administration (FDA, the Agency, or we) is announcing the availability of a guidance for industry entitled “Laboratory Accreditation for Analyses of Foods: What You Need to Know About the FDA Regulation: Guidance for Industry—<span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>.” The <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) is intended to <span class=\"match\">help</span> <span class=\"match\">small</span> entities comply with the final rule entitled “Laboratory Accreditation for Analyses of Foods.” \n \n \n DATES: \n \n The announcement of the guidance is published in the \n Federal Register \n on October 20, 2022.\n \n \n \n ADDRESSES: "},{"title":"Retirement Security Rule: Definition of an Investment Advice Fiduciary","type":"Rule","abstract":"The Department of Labor (Department) is adopting a final rule defining when a person renders \"investment advice for a fee or other compensation, direct or indirect\" with respect to any moneys or other property of an employee benefit plan, for purposes of the definition of a \"fiduciary\" in the Employee Retirement Income Security Act of 1974 (Title I of ERISA or the Act). The final rule also applies for purposes of Title II of ERISA to the definition of a fiduciary of a plan defined in Internal Revenue Code (Code), including an individual retirement account or other plan identified in the Code. The Department also is publishing elsewhere in this issue of the Federal Register amendments to Prohibited Transaction Exemption 2020-02 (Improving Investment Advice for Workers & Retirees) and to several other existing administrative exemptions from the prohibited transaction rules applicable to fiduciaries under Title I and Title II of ERISA.","document_number":"2024-08065","html_url":"https://www.federalregister.gov/documents/2024/04/25/2024-08065/retirement-security-rule-definition-of-an-investment-advice-fiduciary","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2024-04-25/pdf/2024-08065.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2024-08065.pdf?1713962724","publication_date":"2024-04-25","agencies":[{"raw_name":"DEPARTMENT OF LABOR","name":"Labor Department","id":271,"url":"https://www.federalregister.gov/agencies/labor-department","json_url":"https://www.federalregister.gov/api/v1/agencies/271","parent_id":null,"slug":"labor-department"},{"raw_name":"Employee Benefits Security Administration","name":"Employee Benefits Security Administration","id":131,"url":"https://www.federalregister.gov/agencies/employee-benefits-security-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/131","parent_id":271,"slug":"employee-benefits-security-administration"}],"excerpts":"robo-advisers, and 31 non-bank trustees, are considered <span class=\"match\">small</span> entities. For more information, refer to the Affected Entities discussion in the Regulatory Flexibility Act section of this document.\n \n \n \n \n 720 \n   The burden is estimated as follows: [(302 <span class=\"match\">small</span> retail broker-dealers + 85 <span class=\"match\">small</span> SEC-registered retail registered investment advisers + 144 <span class=\"match\">small</span> SEC-registered non-retail registered investment advisers + 2,192 <span class=\"match\">small</span> State-registered retail registered investment advisers + 568 <span class=\"match\">small</span> State-registered non-retail registered investment advisers)"},{"title":"Commodity Pool Operators, Commodity Trading Advisors, and Commodity Pools: Updating the `Qualified Eligible Person' Definition; Adding Minimum Disclosure Requirements for Pools and Trading Programs; Permitting Monthly Account Statements for Funds of Funds; Technical Amendments","type":"Proposed Rule","abstract":"The Commodity Futures Trading Commission (Commission or CFTC) is proposing amendments to certain provisions of its regulations that would: update the Portfolio Requirement thresholds within the \"Qualified Eligible Person\" definition; require commodity pool operators (CPOs) and commodity trading advisors (CTAs) operating pools and trading programs under the applicable Commission regulations to provide certain minimum disclosures to their prospective pool participants and advisory clients; include revisions that are consistent with long-standing Commission exemptive letters addressing the timing of certain pools' periodic financial reporting; and several technical amendments related to the structure of the regulations that are the subject of this proposal.","document_number":"2023-22324","html_url":"https://www.federalregister.gov/documents/2023/10/12/2023-22324/commodity-pool-operators-commodity-trading-advisors-and-commodity-pools-updating-the-qualified","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-10-12/pdf/2023-22324.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-22324.pdf?1697028325","publication_date":"2023-10-12","agencies":[{"raw_name":"COMMODITY FUTURES TRADING COMMISSION","name":"Commodity Futures Trading Commission","id":77,"url":"https://www.federalregister.gov/agencies/commodity-futures-trading-commission","json_url":"https://www.federalregister.gov/api/v1/agencies/77","parent_id":null,"slug":"commodity-futures-trading-commission"}],"excerpts":"reasonable steps to verify their accredited investor status. \n See also \n Registration and <span class=\"match\">Compliance</span> Requirements for Commodity Pool Operators and Commodity Trading Advisors, 83 FR 52902, 52909-11 (Oct. 18, 2018); “Eliminating the Prohibition Against General Solicitation and General Advertising in Rule 506 and Rule 144A Offerings,” A <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>, SEC, \n available at https://www.sec.gov/info/smallbus/<span class=\"match\">secg</span>/general-solicitation-<span class=\"match\">small</span>-entity-<span class=\"match\">compliance</span>-<span class=\"match\">guide</span>. \n When relying on the exemption in Regulation 506(c), offerors today may comfortably"},{"title":"Requirements for Additional Traceability Records for Certain Foods","type":"Rule","abstract":"The Food and Drug Administration (FDA, the Agency, or we) is issuing a final rule establishing additional recordkeeping requirements for persons who manufacture, process, pack, or hold foods the Agency has designated for inclusion on the Food Traceability List (FTL). The final rule adopts provisions requiring these entities to maintain records containing information on critical tracking events in the supply chain for these designated foods, such as initially packing, shipping, receiving, and transforming these foods. The requirements established in the final rule will help the Agency rapidly and effectively identify recipients of foods to prevent or mitigate foodborne illness outbreaks and address credible threats of serious adverse health consequences or death resulting from foods being adulterated or misbranded. We are issuing this regulation in accordance with the FDA Food Safety Modernization Act (FSMA).","document_number":"2022-24417","html_url":"https://www.federalregister.gov/documents/2022/11/21/2022-24417/requirements-for-additional-traceability-records-for-certain-foods","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2022-11-21/pdf/2022-24417.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2022-24417.pdf?1668528919","publication_date":"2022-11-21","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"}],"excerpts":"into <span class=\"match\">compliance</span> with the final rule might pose more challenges for entities with fewer resources and less experience in traceability, and we intend to provide outreach and guidance to <span class=\"match\">help</span> <span class=\"match\">smaller</span> entities understand and comply with the applicable requirements of the final rule. In addition, in accordance with section 204(h) of FSMA, not later than 180 days after promulgation of this final rule we will issue a <span class=\"match\">small</span> entity <span class=\"match\">compliance</span> <span class=\"match\">guide</span> (<span class=\"match\">SECG</span>) that explains the requirements of subpart S in plain language, with the goal of assisting <span class=\"match\">small</span> entities"},{"title":"Retirement Security Rule: Definition of an Investment Advice Fiduciary","type":"Proposed Rule","abstract":"This document contains a proposed amendment to the regulation defining when a person renders \"investment advice for a fee or other compensation, direct or indirect\" with respect to any moneys or other property of an employee benefit plan, for purposes of the definition of a \"fiduciary\" in the Employee Retirement Income Security Act of 1974 (Title I of ERISA or the Act). The proposal also would amend the parallel regulation defining for purposes of Title II of ERISA, a \"fiduciary\" of a plan defined in Internal Revenue Code (Code) section 4975, including an individual retirement account. The Department also is publishing elsewhere in today's Federal Register proposed amendments to Prohibited Transaction Exemption 2020-02 (Improving Investment Advice for Workers & Retirees) and to several other existing administrative exemptions from the prohibited transaction rules applicable to fiduciaries under Title I and Title II of ERISA.","document_number":"2023-23779","html_url":"https://www.federalregister.gov/documents/2023/11/03/2023-23779/retirement-security-rule-definition-of-an-investment-advice-fiduciary","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2023-11-03/pdf/2023-23779.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2023-23779.pdf?1698929122","publication_date":"2023-11-03","agencies":[{"raw_name":"DEPARTMENT OF LABOR","name":"Labor Department","id":271,"url":"https://www.federalregister.gov/agencies/labor-department","json_url":"https://www.federalregister.gov/api/v1/agencies/271","parent_id":null,"slug":"labor-department"},{"raw_name":"Employee Benefits Security Administration","name":"Employee Benefits Security Administration","id":131,"url":"https://www.federalregister.gov/agencies/employee-benefits-security-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/131","parent_id":271,"slug":"employee-benefits-security-administration"}],"excerpts":"(2017), predicted that “<span class=\"match\">smaller</span> investors will be offered robo-investing type account services and that these <span class=\"match\">small</span>, often entry level, novice investors would lose access to personalized financial planning.” \n 441 \n \n According to a survey conducted by the Insured Retirement Institute, 70 percent of respondents either already had or were considering exiting <span class=\"match\">smaller</span> markets such as <span class=\"match\">small</span> employer-based plans and lower balance IRAs.\n 442 \n \n In another survey, two-thirds of responding advisers said they believed that <span class=\"match\">small</span> investors would have less"},{"title":"Federal Acquisition Regulation; Federal Acquisition Circular 2021-04; Small Entity Compliance Guide","type":"Rule","abstract":"This document is issued under the joint authority of DOD, GSA, and NASA. This Small Entity Compliance Guide has been prepared in accordance with section 212 of the Small Business Regulatory Enforcement Fairness Act of 1996. It consists of a summary of the rule appearing in Federal Acquisition Circular (FAC) 2021-04, which amends the Federal Acquisition Regulation (FAR). Interested parties may obtain further information regarding this rule by referring to FAC 2021-04, which precedes this document.","document_number":"2021-00711","html_url":"https://www.federalregister.gov/documents/2021/01/19/2021-00711/federal-acquisition-regulation-federal-acquisition-circular-2021-04-small-entity-compliance-guide","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2021-01-19/pdf/2021-00711.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2021-00711.pdf?1610718328","publication_date":"2021-01-19","agencies":[{"raw_name":"DEPARTMENT OF DEFENSE","name":"Defense Department","id":103,"url":"https://www.federalregister.gov/agencies/defense-department","json_url":"https://www.federalregister.gov/api/v1/agencies/103","parent_id":null,"slug":"defense-department"},{"raw_name":"GENERAL SERVICES ADMINISTRATION","name":"General Services Administration","id":210,"url":"https://www.federalregister.gov/agencies/general-services-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/210","parent_id":null,"slug":"general-services-administration"},{"raw_name":"NATIONAL AERONAUTICS AND SPACE ADMINISTRATION","name":"National Aeronautics and Space Administration","id":301,"url":"https://www.federalregister.gov/agencies/national-aeronautics-and-space-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/301","parent_id":null,"slug":"national-aeronautics-and-space-administration"}],"excerpts":"ACTION: \n <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>. \n \n \n SUMMARY: \n \n This document is issued under the joint authority of DOD, GSA, and NASA. This \n <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span> \n has been prepared in accordance with section 212 of the <span class=\"match\">Small</span> Business Regulatory Enforcement Fairness Act of 1996. It consists of a summary of the rule appearing in Federal Acquisition Circular (FAC) 2021-04, which amends the Federal Acquisition Regulation (FAR). Interested parties may obtain further information regarding this rule by referring to FAC 2021-04, which precedes"},{"title":"Federal Acquisition Regulation; Federal Acquisition Circular 2021-04; Introduction","type":"Rule","abstract":"This document summarizes the Federal Acquisition Regulation (FAR) rule agreed to by the Civilian Agency Acquisition Council and the Defense Acquisition Regulations Council (Councils) in this Federal Acquisition Circular (FAC) 2021-04. A companion document, the Small Entity Compliance Guide (SECG), follows this FAC.","document_number":"2021-00708","html_url":"https://www.federalregister.gov/documents/2021/01/19/2021-00708/federal-acquisition-regulation-federal-acquisition-circular-2021-04-introduction","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2021-01-19/pdf/2021-00708.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2021-00708.pdf?1610718328","publication_date":"2021-01-19","agencies":[{"raw_name":"DEPARTMENT OF DEFENSE","name":"Defense Department","id":103,"url":"https://www.federalregister.gov/agencies/defense-department","json_url":"https://www.federalregister.gov/api/v1/agencies/103","parent_id":null,"slug":"defense-department"},{"raw_name":"GENERAL SERVICES ADMINISTRATION","name":"General Services Administration","id":210,"url":"https://www.federalregister.gov/agencies/general-services-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/210","parent_id":null,"slug":"general-services-administration"},{"raw_name":"NATIONAL AERONAUTICS AND SPACE ADMINISTRATION","name":"National Aeronautics and Space Administration","id":301,"url":"https://www.federalregister.gov/agencies/national-aeronautics-and-space-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/301","parent_id":null,"slug":"national-aeronautics-and-space-administration"}],"excerpts":"document summarizes the Federal Acquisition Regulation (FAR) rule agreed to by the Civilian Agency Acquisition Council and the Defense Acquisition Regulations Council (Councils) in this Federal Acquisition Circular (FAC) 2021-04. A companion document, the \n <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span> \n (<span class=\"match\">SECG</span>), follows this FAC.\n \n \n \n DATES: \n For effective dates see the separate documents, which follow. \n \n \n FOR FURTHER INFORMATION CONTACT: \n \n Ms. Zenaida Delgado, Procurement Analyst, at 202-969-7207 or \n zenaida.delgado@gsa.gov \n for clarification of content"},{"title":"Withdrawing Rule on Securing Updated and Necessary Statutory Evaluations Timely","type":"Rule","abstract":"The Department of Health and Human Services (HHS or Department) is issuing a final rule withdrawing a rule entitled \"Securing Updated and Necessary Statutory Evaluations Timely\" (SUNSET final rule), which published in the Federal Register of January 19, 2021. The SUNSET final rule was originally scheduled to take effect on March 22, 2021. However, after a lawsuit was filed on March 9, 2021, seeking to overturn the SUNSET final rule, HHS extended the effective date of the SUNSET final rule until September 22, 2022. HHS is now withdrawing the SUNSET final rule.","document_number":"2022-11477","html_url":"https://www.federalregister.gov/documents/2022/05/27/2022-11477/withdrawing-rule-on-securing-updated-and-necessary-statutory-evaluations-timely","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2022-05-27/pdf/2022-11477.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2022-11477.pdf?1653569128","publication_date":"2022-05-27","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"},{"raw_name":"Public Health Service","name":"Public Health Service","id":442,"url":"https://www.federalregister.gov/agencies/public-health-service","json_url":"https://www.federalregister.gov/api/v1/agencies/442","parent_id":221,"slug":"public-health-service"},{"raw_name":"Centers for Medicare and Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"},{"raw_name":"Office of the Inspector General"},{"raw_name":"Office of the Secretary"},{"raw_name":"Administration for Children and Families","name":"Children and Families Administration","id":49,"url":"https://www.federalregister.gov/agencies/children-and-families-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/49","parent_id":221,"slug":"children-and-families-administration"}],"excerpts":"Public Health Service Act. \n \n \n RFA \n Regulatory Flexibility Act. \n \n \n RIA \n Regulatory Impact Analysis. \n \n \n SAMHSA \n Substance Abuse and Mental Health Services Administration. \n \n \n SBA \n <span class=\"match\">Small</span> Business Administration. \n \n \n SEISNOSE \n Significant Economic Impact Upon a Substantial Number of <span class=\"match\">Small</span> Entities. \n \n \n <span class=\"match\">SECG</span> \n <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>. \n \n \n SSA \n Social Security Act. \n \n \n SUNSET \n Securing Updated and Necessary Statutory Evaluations Timely. \n \n \n Unified Agenda \n Unified Agenda of Regulatory and Deregulatory Actions. \n \n \n"},{"title":"Securing Updated and Necessary Statutory Evaluations Timely; Proposal To Withdraw or Repeal","type":"Proposed Rule","abstract":"The Department of Health and Human Services (HHS or Department) is proposing to withdraw or repeal a final rule entitled \"Securing Updated and Necessary Statutory Evaluations Timely\" (SUNSET final rule) and published in the Federal Register of January 19, 2021. The SUNSET final rule was originally scheduled to take effect on March 22, 2021. However, after a lawsuit was filed on March 9, 2021, seeking to overturn the SUNSET final rule, HHS issued an administrative delay of effective date that extended the effective date of the SUNSET final rule until March 22, 2022. HHS is now proposing to withdraw or repeal the SUNSET final rule.","document_number":"2021-23472","html_url":"https://www.federalregister.gov/documents/2021/10/29/2021-23472/securing-updated-and-necessary-statutory-evaluations-timely-proposal-to-withdraw-or-repeal","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2021-10-29/pdf/2021-23472.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2021-23472.pdf?1635425124","publication_date":"2021-10-29","agencies":[{"raw_name":"DEPARTMENT OF HEALTH AND HUMAN SERVICES","name":"Health and Human Services Department","id":221,"url":"https://www.federalregister.gov/agencies/health-and-human-services-department","json_url":"https://www.federalregister.gov/api/v1/agencies/221","parent_id":null,"slug":"health-and-human-services-department"},{"raw_name":"Food and Drug Administration","name":"Food and Drug Administration","id":199,"url":"https://www.federalregister.gov/agencies/food-and-drug-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/199","parent_id":221,"slug":"food-and-drug-administration"},{"raw_name":"Public Health Service","name":"Public Health Service","id":442,"url":"https://www.federalregister.gov/agencies/public-health-service","json_url":"https://www.federalregister.gov/api/v1/agencies/442","parent_id":221,"slug":"public-health-service"},{"raw_name":"Centers for Medicare and Medicaid Services","name":"Centers for Medicare & Medicaid Services","id":45,"url":"https://www.federalregister.gov/agencies/centers-for-medicare-medicaid-services","json_url":"https://www.federalregister.gov/api/v1/agencies/45","parent_id":221,"slug":"centers-for-medicare-medicaid-services"},{"raw_name":"Office of the Inspector General"},{"raw_name":"Office of the Secretary"},{"raw_name":"Administration for Children and Families","name":"Children and Families Administration","id":49,"url":"https://www.federalregister.gov/agencies/children-and-families-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/49","parent_id":221,"slug":"children-and-families-administration"}],"excerpts":"PDV \n Present Daily Value. \n \n \n PHS Act \n Public Health Service Act. \n \n \n RFA \n Regulatory Flexibility Act. \n \n \n SAMSHA \n Substance Abuse and Mental Health Services Administration. \n \n \n SBA \n <span class=\"match\">Small</span> Business Administration. \n \n \n SEISNOSE \n Significant Economic Impact Upon a Substantial Number of <span class=\"match\">Small</span> Entities. \n \n \n <span class=\"match\">SECG</span> \n <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>. \n \n \n SUNSET \n Securing Updated and Necessary Statutory Evaluations Timely. \n \n \n UA \n Unified Agenda. \n \n \n III. Background \n The SUNSET final rule, if implemented, would significantly alter the"},{"title":"Amendments to Class Prohibited Transaction Exemptions To Remove Credit Ratings Pursuant to the Dodd-Frank Wall Street Reform and Consumer Protection Act","type":"Notice","abstract":"This document amends six class exemptions from prohibited transaction rules set forth in the Employee Retirement Income Security Act of 1974 (ERISA or the Act) and the Internal Revenue Code (the Code). The amended exemptions are Prohibited Transaction Exemptions (PTEs) 75-1, 80-83, 81-8, 95-60, 97-41 and 2006-16. The amendments relate to the use of credit ratings as conditions in these class exemptions. Section 939A of the Dodd-Frank Wall Street Reform and Consumer Protection Act requires the Department to remove any references to or requirements of reliance on credit ratings from its class exemptions and to substitute standards of creditworthiness as the Department determines to be appropriate. The amendments affect participants and beneficiaries of employee benefit plans, owners of individual retirement accounts (IRAs), fiduciaries of employee benefit plans and IRAs, and the financial institutions that engage in transactions with, or provide services or products to, the plans and IRAs.","document_number":"2022-04866","html_url":"https://www.federalregister.gov/documents/2022/03/08/2022-04866/amendments-to-class-prohibited-transaction-exemptions-to-remove-credit-ratings-pursuant-to-the","pdf_url":"https://www.govinfo.gov/content/pkg/FR-2022-03-08/pdf/2022-04866.pdf","public_inspection_pdf_url":"https://public-inspection.federalregister.gov/2022-04866.pdf?1646660733","publication_date":"2022-03-08","agencies":[{"raw_name":"DEPARTMENT OF LABOR","name":"Labor Department","id":271,"url":"https://www.federalregister.gov/agencies/labor-department","json_url":"https://www.federalregister.gov/api/v1/agencies/271","parent_id":null,"slug":"labor-department"},{"raw_name":"Employee Benefits Security Administration","name":"Employee Benefits Security Administration","id":131,"url":"https://www.federalregister.gov/agencies/employee-benefits-security-administration","json_url":"https://www.federalregister.gov/api/v1/agencies/131","parent_id":271,"slug":"employee-benefits-security-administration"}],"excerpts":"Statistical Rating Organizations: A <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>, Feb. 4, 2014, available at \n https://www.sec.gov/info/smallbus/<span class=\"match\">secg</span>/5b-3-<span class=\"match\">small</span>-entity-<span class=\"match\">compliance</span>-guide.htm. \n \n \n \n \n 23 \n  66 FR 36156, 36161 (July 11, 2001).\n \n \n \n \n 24 \n  79 FR 1316, 1329 (January 8, 2014) (amending 17 CFR 270.5b-3(c)(1)(iv)(C)(1)).\n \n \n \n \n 25 \n  \n Id. \n at 1329, (amending 17 CFR 270.5b-3(c)(1)(iv)(C)(2)).\n \n \n \n \n 26 \n  See References to Ratings of Nationally Recognized Statistical Rating Organizations: A <span class=\"match\">Small</span> Entity <span class=\"match\">Compliance</span> <span class=\"match\">Guide</span>, Feb. 4, 2014, available at "}]}