Übersicht Gesetze und Rechtstexte US - CFR Title 21: Food and Drugs

US - CFR Title 21: Food and Drugs

Neueste gefundene Änderungen

PART 99—DISSEMINATION OF INFORMATION ON UNAPPROVED/NEW USES FOR MARKETED DRUGS, BIOLOGICS, AND DEVICES 21 CFR Part 99	08.08.2026
PART 900—MAMMOGRAPHY 21 CFR Part 900	08.08.2026
PART 898—PERFORMANCE STANDARD FOR ELECTRODE LEAD WIRES AND PATIENT CABLES 21 CFR Part 898	08.08.2026
PART 895—BANNED DEVICES 21 CFR Part 895	08.08.2026
PART 892—RADIOLOGY DEVICES 21 CFR Part 892	08.08.2026
PART 890—PHYSICAL MEDICINE DEVICES 21 CFR Part 890	08.08.2026
PART 888—ORTHOPEDIC DEVICES 21 CFR Part 888	08.08.2026

Alle Rechtstexte

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 04.03.2026
PART 209—REQUIREMENT FOR AUTHORIZED DISPENSERS AND PHARMACIES TO DISTRIBUTE A SIDE EFFECTS STATEMENT 21 CFR Part 209 28.11.2016
PART 20—PUBLIC INFORMATION 21 CFR Part 20 13.07.2023
PART 210—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL 21 CFR Part 210 17.12.2025
PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS 21 CFR Part 211 17.12.2025
PART 212—CURRENT GOOD MANUFACTURING PRACTICE FOR POSITRON EMISSION TOMOGRAPHY DRUGS 21 CFR Part 212 28.11.2016
PART 213—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICAL GASES 21 CFR Part 213 17.12.2025
PART 216—HUMAN DRUG COMPOUNDING 21 CFR Part 216 20.03.2019
PART 21—PROTECTION OF PRIVACY 21 CFR Part 21 28.12.2016
PART 225—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS 21 CFR Part 225 28.11.2016
PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES 21 CFR Part 226 28.11.2016
PART 230—CERTIFICATION AND POSTMARKETING REPORTING FOR DESIGNATED MEDICAL GASES 21 CFR Part 230 17.12.2025
PART 250—SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS 21 CFR Part 250 28.11.2016
PART 251—SECTION 804 IMPORTATION PROGRAM 21 CFR Part 251 29.11.2020
PART 25—ENVIRONMENTAL IMPACT CONSIDERATIONS 21 CFR Part 25 13.07.2023
PART 290—CONTROLLED DRUGS 21 CFR Part 290 28.11.2016
PART 299—DRUGS; OFFICIAL NAMES AND ESTABLISHED NAMES 21 CFR Part 299 28.11.2016
PART 2—GENERAL ADMINISTRATIVE RULINGS AND DECISIONS 21 CFR Part 2 22.03.2026
PART 300—GENERAL 21 CFR Part 300 13.11.2022
PART 310—NEW DRUGS 21 CFR Part 310 15.11.2020

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