Monitoring Gesetzessammlung

Gesetze und Verordnungen US - CFR Title 21: Food and Drugs alphabetisch

A B C D E F G H I J
K L M N O P Q R S T
U V W X Y Z
0 1 2 3 4 5 6 7 8 9
PART 205—GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS
21 CFR Part 205
PART 206—IMPRINTING OF SOLID ORAL DOSAGE FORM DRUG PRODUCTS FOR HUMAN USE
21 CFR Part 206
PART 207—REQUIREMENTS FOR FOREIGN AND DOMESTIC ESTABLISHMENT REGISTRATION AND LISTING FOR HUMAN DRUGS, INCLUDING DRUGS THAT ARE REGULATED UNDER A BIOLOGICS LICENSE APPLICATION, AND ANIMAL DRUGS, AND THE NATIONAL DRUG CODE
21 CFR Part 207
PART 209—REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT
21 CFR Part 209
PART 21—PROTECTION OF PRIVACY
21 CFR Part 21
PART 210—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
21 CFR Part 210
PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
21 CFR Part 211
PART 212—CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS
21 CFR Part 212
PART 213—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICAL GASES
21 CFR Part 213
PART 216—HUMAN DRUG COMPOUNDING
21 CFR Part 216
PART 225—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
21 CFR Part 225
PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
21 CFR Part 226
PART 230—CERTIFICATION AND POSTMARKETING REPORTING FOR DESIGNATED MEDICAL GASES
21 CFR Part 230
PART 25—ENVIRONMENTAL IMPACT CONSIDERATIONS
21 CFR Part 25
PART 250—SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS
21 CFR Part 250
PART 251—SECTION 804 IMPORTATION PROGRAM
21 CFR Part 251
PART 290—CONTROLLED DRUGS
21 CFR Part 290
PART 299—DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES
21 CFR Part 299
PART 3—PRODUCT JURISDICTION
21 CFR Part 3
PART 300—GENERAL
21 CFR Part 300
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