Get notified when this
CFR title is updated:
TITLE 21 : FOOD AND DRUGS [ 21 CFR ]
Note:
— Current as of: 09/27/2012
— Enhanced with links to US Code and FR Reference where ever possible and more to come.
— This consolidated CFR title was last updated by Federal Register (FR) dated 09/14/2012 for Part 520.
— Click here to check the important dates mentioned in this CFR title (within +/- 30 days).New
— Additional Federal Register entries were published for this title after the current date mentioned above. Click here to view these FR entries.
|
— PART 1 : GENERAL ENFORCEMENT REGULATIONS [ 21 CFR 1 ] [Last FR Update:23-Feb-2012]
— PART 2 : GENERAL ADMINISTRATIVE RULINGS AND DECISIONS [ 21 CFR 2 ] [Last FR Update:14-Apr-2010]
— PART 3 : PRODUCT JURISDICTION [ 21 CFR 3 ] [Last FR Update:23-Mar-2010]
— PART 5 : ORGANIZATION [ 21 CFR 5 ] [Last FR Update:19-Mar-2012]
— PART 7 : ENFORCEMENT POLICY [ 21 CFR 7 ] [Last FR Update:02-Feb-2012]
— PART 10 : ADMINISTRATIVE PRACTICES AND PROCEDURES [ 21 CFR 10 ] [Last FR Update:01-Jun-2011]
— PART 11 : ELECTRONIC RECORDS; ELECTRONIC SIGNATURES [ 21 CFR 11 ] [Last FR Update:09-Dec-2004]
— PART 12 : FORMAL EVIDENTIARY PUBLIC HEARING [ 21 CFR 12 ] [Last FR Update:09-May-2003]
— PART 13 : PUBLIC HEARING BEFORE A PUBLIC BOARD OF INQUIRY [ 21 CFR 13 ] [Last FR Update:03-Mar-1989]
— PART 14 : PUBLIC HEARING BEFORE A PUBLIC ADVISORY COMMITTEE [ 21 CFR 14 ] [Last FR Update:01-Jun-2011]
— PART 15 : PUBLIC HEARING BEFORE THE COMMISSIONER [ 21 CFR 15 ] [Last FR Update:18-Jun-1982]
— PART 16 : REGULATORY HEARING BEFORE THE FOOD AND DRUG ADMINISTRATION [ 21 CFR 16 ] [Last FR Update:09-Jul-2009]
— PART 17 : CIVIL MONEY PENALTIES HEARINGS [ 21 CFR 17 ] [Last FR Update:30-Nov-2010]
— PART 19 : STANDARDS OF CONDUCT AND CONFLICTS OF INTEREST [ 21 CFR 19 ] [Last FR Update:01-Jun-2011]
— PART 20 : PUBLIC INFORMATION [ 21 CFR 20 ] [Last FR Update:01-Jun-2011]
— PART 21 : PROTECTION OF PRIVACY [ 21 CFR 21 ] [Last FR Update:01-Jun-2011]
— PART 25 : ENVIRONMENTAL IMPACT CONSIDERATIONS [ 21 CFR 25 ] [Last FR Update:26-Sep-2011]
— PART 26 : MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STATES AND THE EUROPEAN COMMUNITY [ 21 CFR 26 ] [Last FR Update:26-Mar-2009]
— PART 50 : PROTECTION OF HUMAN SUBJECTS [ 21 CFR 50 ] [Last FR Update:24-Jun-2011]
— PART 54 : FINANCIAL DISCLOSURE BY CLINICAL INVESTIGATORS [ 21 CFR 54 ] [Last FR Update:05-Jan-1999]
— PART 56 : INSTITUTIONAL REVIEW BOARDS [ 21 CFR 56 ] [Last FR Update:15-Jan-2009]
— PART 58 : GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES [ 21 CFR 58 ] [Last FR Update:21-May-2002]
— PART 60 : PATENT TERM RESTORATION [ 21 CFR 60 ] [Last FR Update:04-Mar-2002]
— PART 70 : COLOR ADDITIVES [ 21 CFR 70 ] [Last FR Update:06-Nov-2001]
— PART 71 : COLOR ADDITIVE PETITIONS [ 21 CFR 71 ] [Last FR Update:06-Nov-2001]
— PART 73 : LISTING OF COLOR ADDITIVES EXEMPT FROM CERTIFICATION [ 21 CFR 73 ] [Last FR Update:04-May-2011]
— PART 74 : LISTING OF COLOR ADDITIVES SUBJECT TO CERTIFICATION [ 21 CFR 74 ] [Last FR Update:06-Jul-2012]
— PART 80 : COLOR ADDITIVE CERTIFICATION [ 21 CFR 80 ] [Last FR Update:07-Dec-2006]
— PART 81 : GENERAL SPECIFICATIONS AND GENERAL RESTRICTIONS FOR PROVISIONAL COLOR ADDITIVES FOR USE IN FOODS, DRUGS, AND COSMETICS [ 21 CFR 81 ] [Last FR Update:21-Aug-1979]
— PART 82 : LISTING OF CERTIFIED PROVISIONALLY LISTED COLORS AND SPECIFICATIONS [ 21 CFR 82 ] [Last FR Update:30-Aug-1988]
— PART 99 : DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES [ 21 CFR 99 ] [Last FR Update:24-Mar-2005]
— PART 100 : GENERAL [ 21 CFR 100 ] [Last FR Update:06-Nov-2001]
— PART 101 : FOOD LABELING [ 21 CFR 101 ] [Last FR Update:05-Jan-2009]
— PART 102 : COMMON OR USUAL NAME FOR NONSTANDARDIZED FOODS [ 21 CFR 102 ] [Last FR Update:06-Nov-2001]
— PART 104 : NUTRITIONAL QUALITY GUIDELINES FOR FOODS [ 21 CFR 104 ] [Last FR Update:27-Mar-1998]
— PART 105 : FOODS FOR SPECIAL DIETARY USE [ 21 CFR 105 ] [Last FR Update:06-Jan-1993]
— PART 106 : INFANT FORMULA QUALITY CONTROL PROCEDURES [ 21 CFR 106 ] [Last FR Update:09-Jun-2010]
— PART 107 : INFANT FORMULA [ 21 CFR 107 ] [Last FR Update:09-Jun-2010]
— PART 108 : EMERGENCY PERMIT CONTROL [ 21 CFR 108 ] [Last FR Update:06-Nov-2001]
— PART 109 : UNAVOIDABLE CONTAMINANTS IN FOOD FOR HUMAN CONSUMPTION AND FOOD-PACKAGING MATERIAL [ 21 CFR 109 ] [Last FR Update:06-Nov-2001]
— PART 110 : CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKING, OR HOLDING HUMAN FOOD [ 21 CFR 110 ] [Last FR Update:06-Nov-2001]
— PART 111 : CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS [ 21 CFR 111 ] [Last FR Update:14-May-2008]
— PART 113 : THERMALLY PROCESSED LOW-ACID FOODS PACKAGED IN HERMETICALLY SEALED CONTAINERS [ 21 CFR 113 ] [Last FR Update:28-Dec-2011]
— PART 114 : ACIDIFIED FOODS [ 21 CFR 114 ] [Last FR Update:19-Sep-2000]
— PART 115 : SHELL EGGS [ 21 CFR 115 ] [Last FR Update:05-Dec-2000]
— PART 118 : PRODUCTION, STORAGE, AND TRANSPORTATION OF SHELL EGGS [ 21 CFR 118 ] [Last FR Update:13-Apr-2010]
— PART 119 : DIETARY SUPPLEMENTS THAT PRESENT A SIGNIFICANT OR UNREASONABLE RISK [ 21 CFR 119 ] [Last FR Update:11-Feb-2004]
— PART 120 : HAZARD ANALYSIS AND CRITICAL CONTROL POINT (HACCP) SYSTEMS [ 21 CFR 120 ] [Last FR Update:19-Jan-2001]
— PART 123 : FISH AND FISHERY PRODUCTS [ 21 CFR 123 ] [Last FR Update:18-Dec-1995]
— PART 129 : PROCESSING AND BOTTLING OF BOTTLED DRINKING WATER [ 21 CFR 129 ] [Last FR Update:29-May-2009]
— PART 130 : FOOD STANDARDS: GENERAL [ 21 CFR 130 ] [Last FR Update:06-Nov-2001]
— PART 131 : MILK AND CREAM [ 21 CFR 131 ] [Last FR Update:20-Nov-1996]
— PART 133 : CHEESES AND RELATED CHEESE PRODUCTS [ 21 CFR 133 ] [Last FR Update:24-Mar-1998]
— PART 135 : FROZEN DESSERTS [ 21 CFR 135 ] [Last FR Update:27-Mar-1998]
— PART 136 : BAKERY PRODUCTS [ 21 CFR 136 ] [Last FR Update:24-Mar-1998]
— PART 137 : CEREAL FLOURS AND RELATED PRODUCTS [ 21 CFR 137 ] [Last FR Update:05-Mar-1996]
— PART 139 : MACARONI AND NOODLE PRODUCTS [ 21 CFR 139 ] [Last FR Update:24-Mar-1998]
— PART 145 : CANNED FRUITS [ 21 CFR 145 ] [Last FR Update:24-Mar-1998]
— PART 146 : CANNED FRUIT JUICES [ 21 CFR 146 ] [Last FR Update:30-Mar-2001]
— PART 150 : FRUIT BUTTERS, JELLIES, PRESERVES, AND RELATED PRODUCTS [ 21 CFR 150 ] [Last FR Update:24-Mar-1998]
— PART 152 : FRUIT PIES [ 21 CFR 152 ] [Last FR Update:06-Jan-1993]
— PART 155 : CANNED VEGETABLES [ 21 CFR 155 ] [Last FR Update:24-Mar-1998]
— PART 156 : VEGETABLE JUICES [ 21 CFR 156 ] [Last FR Update:24-Mar-1998]
— PART 158 : FROZEN VEGETABLES [ 21 CFR 158 ] [Last FR Update:06-Jan-1993]
— PART 160 : EGGS AND EGG PRODUCTS [ 21 CFR 160 ] [Last FR Update:24-Mar-1998]
— PART 161 : FISH AND SHELLFISH [ 21 CFR 161 ] [Last FR Update:06-Nov-2001]
— PART 163 : CACAO PRODUCTS [ 21 CFR 163 ] [Last FR Update:04-Oct-2002]
— PART 164 : TREE NUT AND PEANUT PRODUCTS [ 21 CFR 164 ] [Last FR Update:24-Mar-1998]
— PART 165 : BEVERAGES [ 21 CFR 165 ] [Last FR Update:19-Oct-2011]
— PART 166 : MARGARINE [ 21 CFR 166 ] [Last FR Update:24-Mar-1998]
— PART 168 : SWEETENERS AND TABLE SIRUPS [ 21 CFR 168 ] [Last FR Update:24-Mar-1998]
— PART 169 : FOOD DRESSINGS AND FLAVORINGS [ 21 CFR 169 ] [Last FR Update:24-Mar-1998]
— PART 170 : FOOD ADDITIVES [ 21 CFR 170 ] [Last FR Update:08-Mar-2007]
— PART 171 : FOOD ADDITIVE PETITIONS [ 21 CFR 171 ] [Last FR Update:08-Mar-2007]
— PART 172 : FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION [ 21 CFR 172 ] [Last FR Update:29-Aug-2012]
— PART 173 : SECONDARY DIRECT FOOD ADDITIVES PERMITTED IN FOOD FOR HUMAN CONSUMPTION [ 21 CFR 173 ] [Last FR Update:26-Sep-2011]
— PART 174 : INDIRECT FOOD ADDITIVES: GENERAL [ 21 CFR 174 ] [Last FR Update:21-May-2002]
— PART 175 : INDIRECT FOOD ADDITIVES: ADHESIVES AND COMPONENTS OF COATINGS [ 21 CFR 175 ] [Last FR Update:13-Jun-2000]
— PART 176 : INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS [ 21 CFR 176 ] [Last FR Update:04-May-2004]
— PART 177 : INDIRECT FOOD ADDITIVES: POLYMERS [ 21 CFR 177 ] [Last FR Update:17-Jul-2012]
— PART 178 : INDIRECT FOOD ADDITIVES: ADJUVANTS, PRODUCTION AIDS, AND SANITIZERS [ 21 CFR 178 ] [Last FR Update:26-Sep-2011]
— PART 179 : IRRADIATION IN THE PRODUCTION, PROCESSING AND HANDLING OF FOOD [ 21 CFR 179 ] [Last FR Update:11-Jun-2012]
— PART 180 : FOOD ADDITIVES PERMITTED IN FOOD OR IN CONTACT WITH FOOD ON AN INTERIM BASIS PENDING ADDITIONAL STUDY [ 21 CFR 180 ] [Last FR Update:08-Mar-2007]
— PART 181 : PRIOR-SANCTIONED FOOD INGREDIENTS [ 21 CFR 181 ] [Last FR Update:27-Sep-1989]
— PART 182 : SUBSTANCES GENERALLY RECOGNIZED AS SAFE [ 21 CFR 182 ] [Last FR Update:26-Sep-2011]
— PART 184 : DIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE [ 21 CFR 184 ] [Last FR Update:26-Sep-2011]
— PART 186 : INDIRECT FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE [ 21 CFR 186 ] [Last FR Update:04-May-2004]
— PART 189 : SUBSTANCES PROHIBITED FROM USE IN HUMAN FOOD [ 21 CFR 189 ] [Last FR Update:17-Apr-2008]
— PART 190 : DIETARY SUPPLEMENTS [ 21 CFR 190 ] [Last FR Update:30-Mar-2001]
— PART 200 : GENERAL [ 21 CFR 200 ] [Last FR Update:26-May-2000]
— PART 201 : LABELING [ 21 CFR 201 ] [Last FR Update:26-Jul-2011]
— PART 202 : PRESCRIPTION DRUG ADVERTISING [ 21 CFR 202 ] [Last FR Update:06-Dec-2007]
— PART 203 : PRESCRIPTION DRUG MARKETING [ 21 CFR 203 ] [Last FR Update:26-Mar-2009]
— PART 205 : GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS [ 21 CFR 205 ] [Last FR Update:09-Oct-2008]
— PART 206 : IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE [ 21 CFR 206 ] [Last FR Update:26-Mar-2009]
— PART 207 : REGISTRATION OF PRODUCERS OF DRUGS AND LISTING OF DRUGS IN COMMERCIAL DISTRIBUTION [ 21 CFR 207 ] [Last FR Update:06-Dec-2007]
— PART 208 : MEDICATION GUIDES FOR PRESCRIPTION DRUG PRODUCTS [ 21 CFR 208 ] [Last FR Update:03-Jan-2008]
— PART 209 : REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT [ 21 CFR 209 ] [Last FR Update:03-Jan-2008]
— PART 210 : CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL [ 21 CFR 210 ] [Last FR Update:10-Dec-2009]
— PART 211 : CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS [ 21 CFR 211 ] [Last FR Update:20-Mar-2012]
— PART 212 : CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS [ 21 CFR 212 ] [Last FR Update:10-Dec-2009]
— PART 216 : PHARMACY COMPOUNDING [ 21 CFR 216 ] [Last FR Update:08-Mar-1999]
— PART 225 : CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS [ 21 CFR 225 ] [Last FR Update:06-Dec-2007]
— PART 226 : CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES [ 21 CFR 226 ] [Last FR Update:06-Dec-2007]
— PART 250 : SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS [ 21 CFR 250 ] [Last FR Update:08-Apr-2004]
— PART 290 : CONTROLLED DRUGS [ 21 CFR 290 ] [Last FR Update:01-Feb-2002]
— PART 299 : DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES [ 21 CFR 299 ] [Last FR Update:09-Apr-2004]
— PART 300 : GENERAL [ 21 CFR 300 ] [Last FR Update:05-Jan-1999]
— PART 310 : NEW DRUGS [ 21 CFR 310 ] [Last FR Update:26-Mar-2009]
— PART 312 : INVESTIGATIONAL NEW DRUG APPLICATION [ 21 CFR 312 ] [Last FR Update:30-Apr-2012]
— PART 314 : APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG [ 21 CFR 314 ] [Last FR Update:19-Dec-2011]
— PART 315 : DIAGNOSTIC RADIOPHARMACEUTICALS [ 21 CFR 315 ] [Last FR Update:17-May-1999]
— PART 316 : ORPHAN DRUGS [ 21 CFR 316 ] [Last FR Update:13-Aug-2009]
— PART 320 : BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS [ 21 CFR 320 ] [Last FR Update:29-Sep-2010]
— PART 328 : OVER-THE-COUNTER DRUG PRODUCTS INTENDED FOR ORAL INGESTION THAT CONTAIN ALCOHOL [ 21 CFR 328 ] [Last FR Update:09-May-2003]
— PART 330 : OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED [ 21 CFR 330 ] [Last FR Update:09-May-2003]
— PART 331 : ANTACID PRODUCTS FOR OVER-THE-COUNTER (OTC) HUMAN USE [ 21 CFR 331 ] [Last FR Update:24-Mar-2004]
— PART 332 : ANTIFLATULENT PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 332 ] [Last FR Update:05-Mar-1996]
— PART 333 : TOPICAL ANTIMICROBIAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 333 ] [Last FR Update:04-Mar-2010]
— PART 335 : ANTIDIARRHEAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 335 ] [Last FR Update:12-May-2004]
— PART 336 : ANTIEMETIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 336 ] [Last FR Update:06-Dec-2003]
— PART 338 : NIGHTTIME SLEEP-AID DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 338 ] [Last FR Update:06-Dec-2002]
— PART 340 : STIMULANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 340 ] [Last FR Update:29-Feb-1988]
— PART 341 : COLD, COUGH, ALLERGY, BRONCHODILATOR, AND ANTIASTHMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 341 ] [Last FR Update:26-Jul-2011]
— PART 343 : INTERNAL ANALGESIC, ANTIPYRETIC, AND ANTIRHEUMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 343 ] [Last FR Update:14-Sep-1999]
— PART 344 : TOPICAL OTIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 344 ] [Last FR Update:10-Aug-2000]
— PART 346 : ANORECTAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 346 ] [Last FR Update:17-Mar-1999]
— PART 347 : SKIN PROTECTANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 347 ] [Last FR Update:06-Mar-2009]
— PART 348 : EXTERNAL ANALGESIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 348 ] [Last FR Update:19-Jun-1992]
— PART 349 : OPHTHALMIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 349 ] [Last FR Update:03-Jun-2003]
— PART 350 : ANTIPERSPIRANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 350 ] [Last FR Update:01-Jun-2011]
— PART 352 : SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY] [ 21 CFR 352 ] [Last FR Update:04-Jun-2003]
— PART 355 : ANTICARIES DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 355 ] [Last FR Update:09-May-2003]
— PART 357 : MISCELLANEOUS INTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 357 ] [Last FR Update:11-May-1990]
— PART 358 : MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [ 21 CFR 358 ] [Last FR Update:06-Mar-2007]
— PART 361 : PRESCRIPTION DRUGS FOR HUMAN USE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED: DRUGS USED IN RESEARCH [ 21 CFR 361 ] [Last FR Update:01-Feb-2002]
— PART 369 : INTERPRETATIVE STATEMENTS RE WARNINGS ON DRUGS AND DEVICES FOR OVER-THE-COUNTER SALE [ 21 CFR 369 ] [Last FR Update:09-Jun-2003]
— PART 500 : GENERAL [ 21 CFR 500 ] [Last FR Update:22-Aug-2012]
— PART 501 : ANIMAL FOOD LABELING [ 21 CFR 501 ] [Last FR Update:03-May-1996]
— PART 502 : COMMON OR USUAL NAMES FOR NONSTANDARDIZED ANIMAL FOODS [ 21 CFR 502 ] [Last FR Update:13-May-1977]
— PART 509 : UNAVOIDABLE CONTAMINANTS IN ANIMAL FOOD AND FOOD-PACKAGING MATERIAL [ 21 CFR 509 ] [Last FR Update:09-May-2003]
— PART 510 : NEW ANIMAL DRUGS [ 21 CFR 510 ] [Last FR Update:06-Dec-2007]
— PART 511 : NEW ANIMAL DRUGS FOR INVESTIGATIONAL USE [ 21 CFR 511 ] [Last FR Update:30-Apr-2012]
— PART 514 : NEW ANIMAL DRUG APPLICATIONS [ 21 CFR 514 ] [Last FR Update:13-Dec-2006]
— PART 515 : MEDICATED FEED MILL LICENSE [ 21 CFR 515 ] [Last FR Update:06-Dec-2007]
— PART 516 : NEW ANIMAL DRUGS FOR MINOR USE AND MINOR SPECIES [ 21 CFR 516 ] [Last FR Update:15-Jun-2012]
— PART 520 : ORAL DOSAGE FORM NEW ANIMAL DRUGS [ 21 CFR 520 ] [Last FR Update:14-Sep-2012]
— PART 522 : IMPLANTATION OR INJECTABLE DOSAGE FORM NEW ANIMAL DRUGS [ 21 CFR 522 ] [Last FR Update:10-Sep-2012]
— PART 524 : OPHTHALMIC AND TOPICAL DOSAGE FORM NEW ANIMAL DRUGS [ 21 CFR 524 ] [Last FR Update:09-Aug-2012]
— PART 526 : INTRAMAMMARY DOSAGE FORM NEW ANIMAL DRUGS [ 21 CFR 526 ] [Last FR Update:29-Mar-2011]
— PART 528 : NEW ANIMAL DRUGS IN GENETICALLY ENGINEERED ANIMALS [ 21 CFR 528 ] [Last FR Update:11-Feb-2009]
— PART 529 : CERTAIN OTHER DOSAGE FORM NEW ANIMAL DRUGS [ 21 CFR 529 ] [Last FR Update:29-Mar-2011]
— PART 530 : EXTRALABEL DRUG USE IN ANIMALS [ 21 CFR 530 ] [Last FR Update:06-Jan-2012]
— PART 556 : TOLERANCES FOR RESIDUES OF NEW ANIMAL DRUGS IN FOOD [ 21 CFR 556 ] [Last FR Update:10-Sep-2012]
— PART 558 : NEW ANIMAL DRUGS FOR USE IN ANIMAL FEEDS [ 21 CFR 558 ] [Last FR Update:31-May-2012]
— PART 570 : FOOD ADDITIVES [ 21 CFR 570 ] [Last FR Update:29-Jul-1997]
— PART 571 : FOOD ADDITIVE PETITIONS [ 21 CFR 571 ] [Last FR Update:29-Jul-1997]
— PART 573 : FOOD ADDITIVES PERMITTED IN FEED AND DRINKING WATER OF ANIMALS [ 21 CFR 573 ] [Last FR Update:09-Feb-2011]
— PART 579 : IRRADIATION IN THE PRODUCTION, PROCESSING, AND HANDLING OF ANIMAL FEED AND PET FOOD [ 21 CFR 579 ] [Last FR Update:10-Apr-2001]
— PART 582 : SUBSTANCES GENERALLY RECOGNIZED AS SAFE [ 21 CFR 582 ] [Last FR Update:02-May-1996]
— PART 584 : FOOD SUBSTANCES AFFIRMED AS GENERALLY RECOGNIZED AS SAFE IN FEED AND DRINKING WATER OF ANIMALS [ 21 CFR 584 ] [Last FR Update:31-Jul-2007]
— PART 589 : SUBSTANCES PROHIBITED FROM USE IN ANIMAL FOOD OR FEED [ 21 CFR 589 ] [Last FR Update:25-Apr-2008]
— PART 600 : BIOLOGICAL PRODUCTS: GENERAL [ 21 CFR 600 ] [Last FR Update:03-May-2012]
— PART 601 : LICENSING [ 21 CFR 601 ] [Last FR Update:05-May-2009]
— PART 606 : CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS [ 21 CFR 606 ] [Last FR Update:03-Jan-2012]
— PART 607 : ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS [ 21 CFR 607 ] [Last FR Update:16-Aug-2007]
— PART 610 : GENERAL BIOLOGICAL PRODUCTS STANDARDS [ 21 CFR 610 ] [Last FR Update:03-May-2012]
— PART 630 : GENERAL REQUIREMENTS FOR BLOOD, BLOOD COMPONENTS, AND BLOOD DERIVATIVES [ 21 CFR 630 ] [Last FR Update:11-Jun-2001]
— PART 640 : ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS [ 21 CFR 640 ] [Last FR Update:03-Jan-2012]
— PART 660 : ADDITIONAL STANDARDS FOR DIAGNOSTIC SUBSTANCES FOR LABORATORY TESTS [ 21 CFR 660 ] [Last FR Update:24-Mar-2005]
— PART 680 : ADDITIONAL STANDARDS FOR MISCELLANEOUS PRODUCTS [ 21 CFR 680 ] [Last FR Update:24-May-2012]
— PART 700 : GENERAL [ 21 CFR 700 ] [Last FR Update:17-Apr-2008]
— PART 701 : COSMETIC LABELING [ 21 CFR 701 ] [Last FR Update:09-Apr-2004]
— PART 710 : VOLUNTARY REGISTRATION OF COSMETIC PRODUCT ESTABLISHMENTS [ 21 CFR 710 ] [Last FR Update:31-Mar-2003]
— PART 720 : VOLUNTARY FILING OF COSMETIC PRODUCT INGREDIENT COMPOSITION STATEMENTS [ 21 CFR 720 ] [Last FR Update:12-May-2003]
— PART 740 : COSMETIC PRODUCT WARNING STATEMENTS [ 21 CFR 740 ] [Last FR Update:24-Mar-2004]
— PART 800 : GENERAL [ 21 CFR 800 ] [Last FR Update:19-Jun-2008]
— PART 801 : LABELING [ 21 CFR 801 ] [Last FR Update:22-Apr-2010]
— PART 803 : MEDICAL DEVICE REPORTING [ 21 CFR 803 ] [Last FR Update:09-Jun-2010]
— PART 806 : MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS [ 21 CFR 806 ] [Last FR Update:10-Mar-2004]
— PART 807 : ESTABLISHMENT REGISTRATION AND DEVICE LISTING FOR MANUFACTURERS AND INITIAL IMPORTERS OF DEVICES [ 21 CFR 807 ] [Last FR Update:22-Apr-2010]
— PART 808 : EXEMPTIONS FROM FEDERAL PREEMPTION OF STATE AND LOCAL MEDICAL DEVICE REQUIREMENTS [ 21 CFR 808 ] [Last FR Update:19-Jun-2008]
— PART 809 : IN VITRO DIAGNOSTIC PRODUCTS FOR HUMAN USE [ 21 CFR 809 ] [Last FR Update:28-Dec-2007]
— PART 810 : MEDICAL DEVICE RECALL AUTHORITY [ 21 CFR 810 ] [Last FR Update:20-Nov-1996]
— PART 812 : INVESTIGATIONAL DEVICE EXEMPTIONS [ 21 CFR 812 ] [Last FR Update:30-Apr-2012]
— PART 814 : PREMARKET APPROVAL OF MEDICAL DEVICES [ 21 CFR 814 ] [Last FR Update:01-Jun-2011]
— PART 820 : QUALITY SYSTEM REGULATION [ 21 CFR 820 ] [Last FR Update:22-Apr-2010]
— PART 821 : MEDICAL DEVICE TRACKING REQUIREMENTS [ 21 CFR 821 ] [Last FR Update:19-Jun-2008]
— PART 822 : POSTMARKET SURVEILLANCE [ 21 CFR 822 ] [Last FR Update:22-Apr-2010]
— PART 860 : MEDICAL DEVICE CLASSIFICATION PROCEDURES [ 21 CFR 860 ] [Last FR Update:22-Apr-2010]
— PART 861 : PROCEDURES FOR PERFORMANCE STANDARDS DEVELOPMENT [ 21 CFR 861 ] [Last FR Update:10-Dec-1992]
— PART 862 : CLINICAL CHEMISTRY AND CLINICAL TOXICOLOGY DEVICES [ 21 CFR 862 ] [Last FR Update:21-Oct-2009]
— PART 864 : HEMATOLOGY AND PATHOLOGY DEVICES [ 21 CFR 864 ] [Last FR Update:30-Nov-2007]
— PART 866 : IMMUNOLOGY AND MICROBIOLOGY DEVICES [ 21 CFR 866 ] [Last FR Update:09-Mar-2012]
— PART 868 : ANESTHESIOLOGY DEVICES [ 21 CFR 868 ] [Last FR Update:23-Jun-2004]
— PART 870 : CARDIOVASCULAR DEVICES [ 21 CFR 870 ] [Last FR Update:22-Jun-2012]
— PART 872 : DENTAL DEVICES [ 21 CFR 872 ] [Last FR Update:04-Aug-2009]
— PART 874 : EAR, NOSE, AND THROAT DEVICES [ 21 CFR 874 ] [Last FR Update:15-Jun-2011]
— PART 876 : GASTROENTEROLOGY-UROLOGY DEVICES [ 21 CFR 876 ] [Last FR Update:19-Jun-2008]
— PART 878 : GENERAL AND PLASTIC SURGERY DEVICES [ 21 CFR 878 ] [Last FR Update:20-Jul-2011]
— PART 880 : GENERAL HOSPITAL AND PERSONAL USE DEVICES [ 21 CFR 880 ] [Last FR Update:15-Feb-2011]
— PART 882 : NEUROLOGICAL DEVICES [ 21 CFR 882 ] [Last FR Update:23-Mar-2012]
— PART 884 : OBSTETRICAL AND GYNECOLOGICAL DEVICES [ 21 CFR 884 ] [Last FR Update:16-Aug-2011]
— PART 886 : OPHTHALMIC DEVICES [ 21 CFR 886 ] [Last FR Update:19-Aug-2011]
— PART 888 : ORTHOPEDIC DEVICES [ 21 CFR 888 ] [Last FR Update:12-Jun-2007]
— PART 890 : PHYSICAL MEDICINE DEVICES [ 21 CFR 890 ] [Last FR Update:19-Jun-2008]
— PART 892 : RADIOLOGY DEVICES [ 21 CFR 892 ] [Last FR Update:05-Nov-2010]
— PART 895 : BANNED DEVICES [ 21 CFR 895 ] [Last FR Update:14-Jul-2000]
— PART 898 : PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES [ 21 CFR 898 ] [Last FR Update:09-May-1997]
— PART 900 : MAMMOGRAPHY [ 21 CFR 900 ] [Last FR Update:22-Apr-2010]
— PART 1000 : GENERAL [ 21 CFR 1000 ] [Last FR Update:27-Mar-1996]
— PART 1002 : RECORDS AND REPORTS [ 21 CFR 1002 ] [Last FR Update:22-Apr-2010]
— PART 1003 : NOTIFICATION OF DEFECTS OR FAILURE TO COMPLY [ 21 CFR 1003 ] [Last FR Update:22-Feb-1985]
— PART 1004 : REPURCHASE, REPAIRS, OR REPLACEMENT OF ELECTRONIC PRODUCTS [ 21 CFR 1004 ] [Last FR Update:22-Mar-1977]
— PART 1005 : IMPORTATION OF ELECTRONIC PRODUCTS [ 21 CFR 1005 ] [Last FR Update:01-Apr-2010]
— PART 1010 : PERFORMANCE STANDARDS FOR ELECTRONIC PRODUCTS: GENERAL [ 21 CFR 1010 ] [Last FR Update:01-Apr-2010]
— PART 1020 : PERFORMANCE STANDARDS FOR IONIZING RADIATION EMITTING PRODUCTS [ 21 CFR 1020 ] [Last FR Update:09-Apr-2007]
— PART 1030 : PERFORMANCE STANDARDS FOR MICROWAVE AND RADIO FREQUENCY EMITTING PRODUCTS [ 21 CFR 1030 ] [Last FR Update:28-Mar-1994]
— PART 1040 : PERFORMANCE STANDARDS FOR LIGHT-EMITTING PRODUCTS [ 21 CFR 1040 ] [Last FR Update:22-Apr-2010]
— PART 1050 : PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATION-EMITTING PRODUCTS [ 21 CFR 1050 ] [Last FR Update:06-Apr-1988]
— PART 1107 : ESTABLISHMENT REGISTRATION, PRODUCT LISTING, AND SUBSTANTIAL EQUIVALENCE REPORTS [ 21 CFR 1107 ] [Last FR Update:05-Jul-2011]
— PART 1140 : CIGARETTES AND SMOKELESS TOBACCO [ 21 CFR 1140 ] [Last FR Update:19-Mar-2010]
— PART 1141 : (-NA-) [ 21 CFR 1141 ]
— PART 1210 : REGULATIONS UNDER THE FEDERAL IMPORT MILK ACT [ 21 CFR 1210 ] [Last FR Update:22-Mar-1977]
— PART 1230 : REGULATIONS UNDER THE FEDERAL CAUSTIC POISON ACT [ 21 CFR 1230 ] [Last FR Update:20-Nov-1973]
— PART 1240 : CONTROL OF COMMUNICABLE DISEASES [ 21 CFR 1240 ] [Last FR Update:18-Aug-2005]
— PART 1250 : INTERSTATE CONVEYANCE SANITATION [ 21 CFR 1250 ] [Last FR Update:06-Nov-2001]
— PART 1270 : HUMAN TISSUE INTENDED FOR TRANSPLANTATION [ 21 CFR 1270 ] [Last FR Update:24-Nov-2004]
— PART 1271 : HUMAN CELLS, TISSUES, AND CELLULAR AND TISSUE-BASED PRODUCTS [ 21 CFR 1271 ] [Last FR Update:24-Mar-2006]
— PART 1300 : DEFINITIONS [ 21 CFR 1300 ] [Last FR Update:30-Jul-2012]
— PART 1301 : REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, AND DISPENSERS OF CONTROLLED SUBSTANCES [ 21 CFR 1301 ] [Last FR Update:15-Mar-2012]
— PART 1302 : LABELING AND PACKAGING REQUIREMENTS FOR CONTROLLED SUBSTANCES [ 21 CFR 1302 ] [Last FR Update:24-Mar-1997]
— PART 1303 : QUOTAS [ 21 CFR 1303 ] [Last FR Update:27-Jan-2012]
— PART 1304 : RECORDS AND REPORTS OF REGISTRANTS [ 21 CFR 1304 ] [Last FR Update:27-Jan-2012]
— PART 1305 : ORDERS FOR SCHEDULE I AND II CONTROLLED SUBSTANCES [ 21 CFR 1305 ] [Last FR Update:27-Jan-2012]
— PART 1306 : PRESCRIPTIONS [ 21 CFR 1306 ] [Last FR Update:31-Mar-2010]
— PART 1307 : MISCELLANEOUS [ 21 CFR 1307 ] [Last FR Update:09-Mar-2010]
— PART 1308 : SCHEDULES OF CONTROLLED SUBSTANCES [ 21 CFR 1308 ] [Last FR Update:15-Dec-2011]
— PART 1309 : REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, IMPORTERS AND EXPORTERS OF LIST I CHEMICALS [ 21 CFR 1309 ] [Last FR Update:15-Mar-2012]
— PART 1310 : RECORDS AND REPORTS OF LISTED CHEMICALS AND CERTAIN MACHINES [ 21 CFR 1310 ] [Last FR Update:27-Jan-2012]
— PART 1311 : REQUIREMENTS FOR ELECTRONIC ORDERS AND PRESCRIPTIONS [ 21 CFR 1311 ] [Last FR Update:31-Mar-2010]
— PART 1312 : IMPORTATION AND EXPORTATION OF CONTROLLED SUBSTANCES [ 21 CFR 1312 ] [Last FR Update:27-Jan-2012]
— PART 1313 : IMPORTATION AND EXPORTATION OF LIST I AND LIST II CHEMICALS [ 21 CFR 1313 ] [Last FR Update:27-Jan-2012]
— PART 1314 : RETAIL SALE OF SCHEDULED LISTED CHEMICAL PRODUCTS [ 21 CFR 1314 ] [Last FR Update:27-Jan-2012]
— PART 1315 : IMPORTATION AND PRODUCTION QUOTAS FOR EPHEDRINE, PSEUDOEPHEDRINE, AND PHENYLPROPANOLAMINE [ 21 CFR 1315 ] [Last FR Update:09-Mar-2010]
— PART 1316 : ADMINISTRATIVE FUNCTIONS, PRACTICES, AND PROCEDURES [ 21 CFR 1316 ] [Last FR Update:27-Jan-2012]
— PART 1321 : DEA MAILING ADDRESSES [ 21 CFR 1321 ] [Last FR Update:09-Mar-2010]
— PART 1401 : PUBLIC AVAILABILITY OF INFORMATION [ 21 CFR 1401 ] [Last FR Update:15-Dec-1999]
— PART 1402 : MANDATORY DECLASSIFICATION REVIEW [ 21 CFR 1402 ] [Last FR Update:24-Nov-1992]
— PART 1403 : UNIFORM ADMINISTRATIVE REQUIREMENTS FOR GRANTS AND COOPERATIVE AGREEMENTS TO STATE AND LOCAL GOVERNMENTS [ 21 CFR 1403 ] [Last FR Update:29-Aug-1997]
— PART 1404 : GOVERNMENTWIDE DEBARMENT AND SUSPENSION (NONPROCUREMENT) [ 21 CFR 1404 ] [Last FR Update:26-Nov-2003]
— PART 1405 : GOVERNMENTWIDE REQUIREMENTS FOR DRUG-FREE WORKPLACE (FINANCIAL ASSISTANCE) [ 21 CFR 1405 ] [Last FR Update:26-Nov-2003]
|
|
|
