Cfr 21, Parts 800 to 1299, Food and Drugs, April 01, 2016 (Volume 8 Of 9) PDF Download
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Author: Office of the Federal Register (Cfr)
Publisher:
ISBN: 9781359980250
Category :
Languages : en
Pages : 870
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Book Description
Code of Federal Regulations Title 21, Volume 8, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as: - Code of Federal Regulations Title 21, Volume 8, April 1, 2016 - CFR Title 21 - CFR 21, Food and Drugs - CFR 21, Parts 800 to 1299, Food and Drugs This volume contains Parts 800 to 1299: - Part 800; GENERAL - Part 801; LABELING - Part 803; MEDICAL DEVICE REPORTING - Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS - Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES - Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS - Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE - Part 810; MEDICAL DEVICE RECALL AUTHORITY - Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS - Part 813; Reserved - Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES - Part 820; QUALITY SYSTEM REGULATION - Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS - Part 822; POSTMARKET SURVEILLANCE - Part 830; UNIQUE DEVICE IDENTIFICATION - Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES - Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT - Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES - Part 864; HEMATOLOGY AND PATHOLOGY DEVICES - Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES - Part 868; ANESTHESIOLOGY DEVICES - Part 870; CARDIOVASCULAR DEVICES - Part 872; DENTAL DEVICES - Part 874; EAR, NOSE, AND THROAT DEVICES - Part 876; GASTROENTEROLOGY-UROLOGY DEVICES - Part 878; GENERAL AND PLASTIC SURGERY DEVICES - Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES - Part 882; NEUROLOGICAL DEVICES - Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES - Part 886; OPHTHALMIC DEVICES - Part 888; ORTHOPEDIC DEVICES - Part 890; PHYSICAL MEDICINE DEVICES - Part 892; RADIOLOGY DEVICES - Part 895; BANNED DEVICES - Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES - Part 900; MAMMOGRAPHY - Part 1000; GENERAL - Part 1002; RECORDS AND REPORTS - Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY - Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS - Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS - Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL - Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS - Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS - Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS - Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS - Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS - Part 1140; CIGARETTES AND SMOKELESS TOBACCO - Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS - Part 1150; USER FEES - Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT - Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT - Part 1240; CONTROL OF COMMUNICABLE DISEASES - Part 1250; INTERSTATE CONVEYANCE SANITATION - Parts 1251-1269; Reserved - Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION - Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS - Parts 1272-1299; Reserved
Author: Office of the Federal Register (Cfr)
Publisher:
ISBN: 9781359980250
Category :
Languages : en
Pages : 870
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Book Description
Code of Federal Regulations Title 21, Volume 8, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as: - Code of Federal Regulations Title 21, Volume 8, April 1, 2016 - CFR Title 21 - CFR 21, Food and Drugs - CFR 21, Parts 800 to 1299, Food and Drugs This volume contains Parts 800 to 1299: - Part 800; GENERAL - Part 801; LABELING - Part 803; MEDICAL DEVICE REPORTING - Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS - Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES - Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS - Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE - Part 810; MEDICAL DEVICE RECALL AUTHORITY - Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS - Part 813; Reserved - Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES - Part 820; QUALITY SYSTEM REGULATION - Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS - Part 822; POSTMARKET SURVEILLANCE - Part 830; UNIQUE DEVICE IDENTIFICATION - Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES - Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT - Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES - Part 864; HEMATOLOGY AND PATHOLOGY DEVICES - Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES - Part 868; ANESTHESIOLOGY DEVICES - Part 870; CARDIOVASCULAR DEVICES - Part 872; DENTAL DEVICES - Part 874; EAR, NOSE, AND THROAT DEVICES - Part 876; GASTROENTEROLOGY-UROLOGY DEVICES - Part 878; GENERAL AND PLASTIC SURGERY DEVICES - Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES - Part 882; NEUROLOGICAL DEVICES - Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES - Part 886; OPHTHALMIC DEVICES - Part 888; ORTHOPEDIC DEVICES - Part 890; PHYSICAL MEDICINE DEVICES - Part 892; RADIOLOGY DEVICES - Part 895; BANNED DEVICES - Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES - Part 900; MAMMOGRAPHY - Part 1000; GENERAL - Part 1002; RECORDS AND REPORTS - Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY - Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS - Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS - Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL - Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS - Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS - Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS - Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS - Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS - Part 1140; CIGARETTES AND SMOKELESS TOBACCO - Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS - Part 1150; USER FEES - Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT - Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT - Part 1240; CONTROL OF COMMUNICABLE DISEASES - Part 1250; INTERSTATE CONVEYANCE SANITATION - Parts 1251-1269; Reserved - Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION - Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS - Parts 1272-1299; Reserved
Author: Office of the Federal Register (Cfr)
Publisher: Regulations Press
ISBN: 9781298709196
Category : Law
Languages : en
Pages : 898
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Book Description
Code of Federal Regulations Title 21, Volume 8, April 1, 2017 contains regulations governing Food and Drugs and may also be referenced as: - Code of Federal Regulations Title 21, Volume 8, April 1, 2017 - CFR Title 21 - CFR 21, Food and Drugs - CFR 21, Parts 800 to 1299, Food and Drugs This volume contains Parts 800 to 1299: - Part 800; GENERAL - Part 801; LABELING - Part 803; MEDICAL DEVICE REPORTING - Part 806; MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS - Part 807; ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES - Part 808; EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS - Part 809; IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE - Part 810; MEDICAL DEVICE RECALL AUTHORITY - Part 812; INVESTIGATIONAL DEVICE EXEMPTIONS - Part 813; Reserved - Part 814; PREMARKET APPROVAL OF MEDICAL DEVICES - Part 820; QUALITY SYSTEM REGULATION - Part 821; MEDICAL DEVICE TRACKING REQUIREMENTS - Part 822; POSTMARKET SURVEILLANCE - Part 830; UNIQUE DEVICE IDENTIFICATION - Part 860; MEDICAL DEVICE CLASSIFICATION PROCEDURES - Part 861; PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT - Part 862; CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES - Part 864; HEMATOLOGY AND PATHOLOGY DEVICES - Part 866; IMMUNOLOGY AND MICROBIOLOGY DEVICES - Part 868; ANESTHESIOLOGY DEVICES - Part 870; CARDIOVASCULAR DEVICES - Part 872; DENTAL DEVICES - Part 874; EAR, NOSE, AND THROAT DEVICES - Part 876; GASTROENTEROLOGY-UROLOGY DEVICES - Part 878; GENERAL AND PLASTIC SURGERY DEVICES - Part 880; GENERAL HOSPITAL AND PERSONAL USE DEVICES - Part 882; NEUROLOGICAL DEVICES - Part 884; OBSTETRICAL AND GYNECOLOGICAL DEVICES - Part 886; OPHTHALMIC DEVICES - Part 888; ORTHOPEDIC DEVICES - Part 890; PHYSICAL MEDICINE DEVICES - Part 892; RADIOLOGY DEVICES - Part 895; BANNED DEVICES - Part 898; PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES - Part 900; MAMMOGRAPHY - Part 1000; GENERAL - Part 1002; RECORDS AND REPORTS - Part 1003; NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY - Part 1004; REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS - Part 1005; IMPORTATION OF ELECTRONIC PRODUCTS - Part 1010; PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL - Part 1020; PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS - Part 1030; PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS - Part 1040; PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS - Part 1050; PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS - Part 1100; TOBACCO PRODUCTS SUBJECT TO FDA AUTHORITY - Part 1105; GENERAL - Part 1105; GENERAL - Part 1107; ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS - Part 1140; CIGARETTES, SMOKELESS TOBACCO, AND COVERED TOBACCO PRODUCTS - Part 1141; CIGARETTE PACKAGE AND ADVERTISING WARNINGS - Part 1143; MINIMUM REQUIRED WARNING STATEMENTS - Part 1150; USER FEES - Part 1210; REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT - Part 1230; REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT - Part 1240; CONTROL OF COMMUNICABLE DISEASES - Part 1250; INTERSTATE CONVEYANCE SANITATION - Parts 1251-1269; Reserved - Part 1270; HUMAN TISSUE INTENDED FOR TRANSPLANTATION - Part 1271; HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS - Parts 1272-1299; Reserved
Author: Office Of The Federal Register (U S )
Publisher: Office of the Federal Register
ISBN: 9780160932762
Category : Business & Economics
Languages : en
Pages : 868
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Book Description
This print ISBN is the U.S. Federal Government Official edition of this title. 21 CFR Parts 800 to 1299 covers the U. S. Food and Drug Administration within the U.S. Department of Health and Human Services. Within this volume, you will find rules, procedures, and regulations pertaining to medical devices, such as cardiovascular devices, dentistry devices, orthopedic, gastroenterology-urology, in vitro, anestheology, and more. Plus, you will find rules, procedures, and regulations relating to mammography quality standards, radiological health, tobacco products, cigarette package advertising warnings, cigarettes and smokeless tobacco, human tissue intended for transplantation, and more. Audiences: medical device producers and marketers, medical practitioners, tobacco proudcers andmarketers, human health researchers and practioners. Healthcare device manufacturers, hosptital radiological and other medical technicians and departments, physicians, nurses, out-patient clinics' personnel, and healthcare policy advocates, tobacco producers and advertisers/marketers as well as human health researchers and practitionersmay be interested in this volume."
Author: Office of The Federal Register, Enhanced by IntraWEB, LLC
Publisher: IntraWEB, LLC and Claitor's Law Publishing
ISBN: 016092345X
Category : Law
Languages : en
Pages : 843
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Book Description
The Code of Federal Regulations Title 21 contains the codified Federal laws and regulations that are in effect as of the date of the publication pertaining to food and drugs, both legal pharmaceuticals and illegal drugs.
Author: Office of the Federal Register (U.S.)
Publisher: Jeffrey Frank Jones
ISBN:
Category :
Languages : en
Pages : 4753
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Book Description
Author: Office of the Federal Register (Cfr)
Publisher:
ISBN: 9781359980243
Category :
Languages : en
Pages : 220
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Book Description
Code of Federal Regulations Title 21, Volume 7, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as: - Code of Federal Regulations Title 21, Volume 7, April 1, 2016 - CFR Title 21 - CFR 21, Food and Drugs - CFR 21, Parts 600 to 799, Food and Drugs This volume contains Parts 600 to 799: - Part 600; BIOLOGICAL PRODUCTS: GENERAL - Part 601; LICENSING - Part 606; CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS - Part 607; ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS - Part 610; GENERAL BIOLOGICAL PRODUCTS STANDARDS - Part 630; REQUIREMENTS FOR BLOOD AND BLOOD COMPONENTS INTENDED FOR TRANSFUSION OR FOR FURTHER MANUFACTURING USE - Part 640; ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS - Part 660; ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS - Part 680; ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS - Part 700; GENERAL - Part 701; COSMETIC LABELING - Part 710; VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS - Part 720; VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS - Part 740; COSMETIC PRODUCT WARNING STATEMENTS - Parts 741-799; Reserved
Author: Office of the Federal Register (Cfr)
Publisher:
ISBN: 9781359980199
Category :
Languages : en
Pages : 754
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Book Description
Code of Federal Regulations Title 21, Volume 2, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as: - Code of Federal Regulations Title 21, Volume 2, April 1, 2016 - CFR Title 21 - CFR 21, Food and Drugs - CFR 21, Parts 100 to 169, Food and Drugs This volume contains Parts 100 to 169: - Part 100; GENERAL - Part 101; FOOD LABELING - Part 102; COMMON OR USUAL NAME FOR NONSTANDARDIZED FOODS - Part 104; NUTRITIONAL QUALITY GUIDELINES FOR FOODS - Part 105; FOODS FOR SPECIAL DIETARY USE - Part 106; INFANT FORMULA REQUIREMENTS PERTAINING TO CURRENT GOOD MANUFACTURING PRACTICE, QUALITY CONTROL PROCEDURES, QUALITY FACTORS, RECORDS AND REPORTS, AND NOTIFICATIONS - Part 107; INFANT FORMULA - Part 108; EMERGENCY PERMIT CONTROL - Part 109; UNAVOIDABLE CONTAMINANTS IN FOOD FOR HUMAN CONSUMPTION AND FOOD-PACKAGING MATERIAL - Part 110; CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKING, OR HOLDING HUMAN FOOD - Part 111; CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS - Part 112; STANDARDS FOR THE GROWING, HARVESTING, PACKING, AND HOLDING OF PRODUCE FOR HUMAN CONSUMPTION - Part 113; THERMALLY PROCESSED LOW-ACID FOODS PACKAGED IN HERMETICALLY SEALED CONTAINERS - Part 114; ACIDIFIED FOODS - Part 115; SHELL EGGS - Part 117; CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND RISK-BASED PREVENTIVE CONTROLS FOR HUMAN FOOD - Part 118; PRODUCTION, STORAGE, AND TRANSPORTATION OF SHELL EGGS - Part 119; DIETARY SUPPLEMENTS THAT PRESENT A SIGNIFICANT OR UNREASONABLE RISK - Part 120; HAZARD ANALYSIS AND CRITICAL CONTROL POINT (HACCP) SYSTEMS - Part 123; FISH AND FISHERY PRODUCTS - Part 129; PROCESSING AND BOTTLING OF BOTTLED DRINKING WATER - Part 130; FOOD STANDARDS: GENERAL - Part 131; MILK AND CREAM - Part 133; CHEESES AND RELATED CHEESE PRODUCTS - Part 135; FROZEN DESSERTS - Part 136; BAKERY PRODUCTS - Part 137; CEREAL FLOURS AND RELATED PRODUCTS - Part 139; MACARONI AND NOODLE PRODUCTS - Part 145; CANNED FRUITS - Part 146; CANNED FRUIT JUICES - Part 150; FRUIT BUTTERS, JELLIES, PRESERVES, AND RELATED PRODUCTS - Part 152; FRUIT PIES - Part 155; CANNED VEGETABLES - Part 156; VEGETABLE JUICES - Part 158; FROZEN VEGETABLES - Part 160; EGGS AND EGG PRODUCTS - Part 161; FISH AND SHELLFISH - Part 163; CACAO PRODUCTS - Part 164; TREE NUT AND PEANUT PRODUCTS - Part 165; BEVERAGES - Part 166; MARGARINE - Part 168; SWEETENERS AND TABLE SIRUPS - Part 169; FOOD DRESSINGS AND FLAVORINGS
Author: Office of the Federal Register (Cfr)
Publisher:
ISBN: 9781359980205
Category :
Languages : en
Pages : 650
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Book Description
Code of Federal Regulations Title 21, Volume 3, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as: - Code of Federal Regulations Title 21, Volume 3, April 1, 2016 - CFR Title 21 - CFR 21, Food and Drugs - CFR 21, Parts 170 to 199, Food and Drugs This volume contains Parts 170 to 199: - Part 170; FOOD ADDITIVES - Part 171; FOOD ADDITIVE PETITIONS - Part 172; FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION - Part 173; SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION - Part 174; INDIRECT FOOD ADDITIVES: GENERAL - Part 175; INDIRECT FOOD ADDITIVES: ADHESIVES AND COMPONENTS OF COATINGS - Part 176; INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS - Part 177; INDIRECT FOOD ADDITIVES: POLYMERS - Part 178; INDIRECT FOOD ADDITIVES: ADJUVANTS, PRODUCTION AIDS, AND SANITIZERS - Part 179; IRRADIATION IN THE PRODUCTION, PROCESSING AND HANDLING OF FOOD - Part 180; FOOD ADDITIVES PERMITTED IN FOOD OR IN CONTACT WITH FOOD ON AN INTERIM BASIS PENDING ADDITIONAL STUDY - Part 181; PRIOR-SANCTIONED FOOD INGREDIENTS - Part 182; SUBSTANCES GENERALLY RECOGNIZED AS SAFE - Part 184; DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE - Part 186; INDIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE - Part 189; SUBSTANCES PROHIBITED FROM USE IN HUMAN FOOD - Part 190; DIETARY SUPPLEMENTS - Parts 191-199; Reserved
Author: United States. Office of the Federal Register
Publisher:
ISBN:
Category : Drugs
Languages : en
Pages : 858
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Book Description
Author: Office of the Federal Register (US)
Publisher: Createspace Independent Publishing Platform
ISBN: 9781978409279
Category :
Languages : en
Pages : 330
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Book Description
"Title 21-FOOD AND DRUGS is composed of nine volumes. The parts in these volumes are arranged in the following order: Parts 1-99, 100-169, 170-199, 200-299, 300-499, 500-599, 600-799, 800-1299 and 1300-end. The first eight volumes, containing parts 1-1299, comprise Chapter I-Food and Drug Administration, Department of Health and Human Services. The ninth volume, containing part 1300 to end, includes Chapter II-Drug Enforcement Administration, Department of Justice, and Chapter III-Office of National Drug Control Policy. The contents of these volumes represent all current regulations codified under this title of the CFR as of April 1, 2017."
