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This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
§ 321 - Definitions; generally
§ 351 - Adulterated drugs and devices
§ 352 - Misbranded drugs and devices
§ 355 - New drugs
§ 357 - Qualification of drug development tools
§ 360b - New animal drugs
§ 371 - Regulations and hearings
§ 374 - Inspection
§ 216 - Regulations
§ 262 - Regulation of biological products
§ 263a - Certification of laboratories
§ 264 - Regulations to control communicable diseases