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Standards Incorporated by Reference (SIBR) Database

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Accessing Standards Incorporated by Reference

This database provides information on standards that have been incorporated by reference into the US Code of Federal Regulations (CFR). To obtain copies of the standards referenced, information should be provided in the referenced CFR section about how to obtain a copy. Alternatively, individuals can check with the standards publisher, a standards resellers or for a limited number of standards used in regulations, consult the American National Standards Institute (ANSI) Incorporated by Reference (IBR) Portal. This portal provides a mechanism for limited and free access to some of the standards that have been incorporated by reference in the U.S. Code of Federal Regulations (CFR).

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Displaying 24301 - 24350 of 27495
Export results (CSV)
Incorporated by (Agency) FR Citation CFR Citation Document Number Document Edition / Year Title of Standard Standard Publishing Organization
Food and Drug Administration 21 CFR 573.460(a)(1)(i) AAFCO Publication 2003 Official Publication Association of American Feed Control Officials, Inc.
Food and Drug Administration 21 CFR 522.2640(a) FDA Publication 2012 Determination of Factor Content in Tylosin by High Performance Liquid Chromatography Food and Drug Administration, U.S. Department of Health and Human Services
Food and Drug Administration 21 CFR 522.2640(a) FDA Publication 2001 Determination of Factor Content in Tylosin by High Performance Liquid Chromatography Food and Drug Administration, U.S. Department of Health and Human Services
Health and Human Services Department 89 FR 51738 21 CFR 514 ISO 9000 2015 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 514 ISO 13485 2016 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 7496 21 CFR 4 ISO 13485:2016(E) 2016 Medical Devices; Quality System Regulation Amendments International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 4 ISO 9000 2015 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 4 ISO 13485 2016 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 7496 21 CFR 4 ISO 9000:2015(E), Clause 3 2015 Medical Devices; Quality System Regulation Amendments International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 314 ISO 13485 2016 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 314 ISO 9000 2015 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Food and Drug Administration 21 CFR 299.4(d) USAN and the USP Dictionary of Drug Names 1985 Guiding Principles for Coining U.S. Adopted Names for Drugs U.S. Pharmacopeial Convention
Food and Drug Administration 21 CFR 26.60(b) ISO Guide 2 1996 Standardization and Related Activities-General Vocabulary of the ISO and IEC International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 230 ISO 9000 2015 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 230 ISO 13485 2016 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 213 ISO 9000 2015 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Food and Drug Administration 21 CFR 211.176 FDA Publication 1989 Procedures for Detecting and Measuring Penicillin Contamination in Drugs Food and Drug Administration, U.S. Department of Health and Human Services
Food and Drug Administration 21 CFR 211.176 FDA Publication 2012 Procedures for Detecting and Measuring Penicillin Contamination in Drugs Food and Drug Administration, U.S. Department of Health and Human Services
Health and Human Services Department 89 FR 51738 21 CFR 211 ISO 13485 2016 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 211 ISO 9000 2015 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 210 ISO 9000 2015 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 210 ISO 13485 2016 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Food and Drug Administration 21 CFR 201.327(i)(1)(iv) ISO 17166 CIE S007/E 2000 Erythemal reference action spectrum and standard erythema dose International Organization for Standardization
Food and Drug Administration 21 CFR 201.327(i)(1)(ii)(C) ISO 17166 CIE S007/E 2000 Erythemal reference action spectrum and standard erythema dose International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 201 ISO 9000 2015 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Health and Human Services Department 89 FR 51738 21 CFR 201 ISO 13485 2016 Current Good Manufacturing Practice, Certification, Postmarketing Safety Reporting, and Labeling Requirements for Certain Medical Gases International Organization for Standardization
Food and Drug Administration 21 CFR 2.19 AOAC Official Methods 1980 Official Methods of Analysis and Supplements AOAC International
Food and Drug Administration 21 CFR 189.5(a)(6) AOAC Method Ca 3a-46 1997 Insoluble Impurities AOAC International
Food and Drug Administration 21 CFR 189.190(c) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 189.180(c) AOAC Journal 1971 Gas Chromatographic Determination of Safrole and Related in Nonalcoholic Beverages: Collaborative, Vol. 54, No. 4, pages 900-902 AOAC International
Food and Drug Administration 21 CFR 189.175(c) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 189.165(c) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 189.155(c) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 189.145(c) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 189.135(c) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 189.130(c) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 189.110(c) AOAC Journal 1973 Flavors and Nonalcoholic Beverages, Vol. 56, No. 5, pages 1281-1283 AOAC International
Food and Drug Administration 21 CFR 184.1985(b) Food Chemicals Codex 1981 Aminopeptidase Enzyme Preparation Derived from Lactococcus Lactis National Academy Press
Food and Drug Administration 21 CFR 184.1979c(b)(2) Food Chemicals Codex 1996 Whey Protein Concentrate National Academy Press
Food and Drug Administration 21 CFR 184.1979c(b)(1) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 184.1979b(b)(2) Food Chemicals Codex 1996 Reduced Minerals Whey National Academy Press
Food and Drug Administration 21 CFR 184.1979b(b)(1) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 184.1979a(b)(2) Food Chemicals Codex 1996 Reduced Lactose Whey National Academy Press
Food and Drug Administration 21 CFR 184.1979a(b)(1) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 184.1979(b)(2) Food Chemicals Codex 1996 Whey National Academy Press
Food and Drug Administration 21 CFR 184.1979(b)(1) AOAC Official Methods 1980 Official Methods of Analysis AOAC International
Food and Drug Administration 21 CFR 184.1978(b) Food Chemicals Codex 1981 Carnauba Wax National Academy Press
Food and Drug Administration 21 CFR 184.1976(b) Food Chemicals Codex 1981 Candelilla Wax National Academy Press
Food and Drug Administration 21 CFR 184.1973(b) Food Chemicals Codex 1981 Beeswax (Yellow and White) National Academy Press
Food and Drug Administration 21 CFR 184.1950(b) Food Chemicals Codex 1981 Vitamin D National Academy Press

DISCLAIMER: Data and information released from the Standards Incorporated by Reference databases at NIST are provided on an "AS IS" basis, without representation or warranty of any kind, including without limitation the warranties of merchantability, fitness for a particular purpose and non-infringement. Data and/or information in this database may contain errors or may be incomplete. Please email [email protected] if you identified missing information or incorrect information. This database is provided by NIST as a public service. Inclusion of records in this database does not represent endorsement or recommendation of standards listed by NIST.

NOTE: This database does not included records related to the Incorporation by Reference for the following: Department of Transportation, Federal Aviation Administration – Airworthiness Directives, State Air Plan Approvals, and Standard Instrumentation Approach Procedures; and the Environmental Protection Agency - State Approval of Air Quality Plans.