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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
This volume of the Code of Federal Regulations addresses the complex regulatory landscape governing Food and Drugs in the United States, specifically focusing on the period up to April 1, 2017. It compiles the official legal requirements and guidelines established by the Office of the Federal Register. The content is organized to provide a comprehensive reference for understanding the rules and standards applicable to various aspects of food and drug administration and oversight.
This compilation serves as an authoritative reference for legal and regulatory professionals, manufacturers, and anyone involved in the food and drug industries. Its value lies in its comprehensive and official compilation of federal regulations, providing a clear framework for compliance. The structured organization by part and subject matter facilitates efficient access to specific legal requirements.
Page Count:
898
Publication Date:
2017-09-19
Publisher:
Creative Media Partners, LLC
ISBN-10:
1298709199
ISBN-13:
9781298709196
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