Federal · Title 21 — Food and Drugs
21 U.S.C. § 377: Revision of United States Pharmacopoeia; development of analysis and mechanical and physical tests
Read the full statutory text
The Secretary, in carrying into effect the provisions of the Federal Food, Drug, and Cosmetic Act [ 21 U.S.C. 301 et seq.], is authorized on and after July 12, 1943 , to cooperate with associations and scientific societies in the revision of the United States Pharmacopoeia and in the development of methods of analysis and mechanical and physical tests necessary to carry out the work of the Food and Drug Administration.
Verify at the official source: Federal legislative text
Facing this? Know exactly what happens next.
MOFRD turns this code section into your situation: the deadlines that apply to you, the forms your county uses, and the resolution paths people in your position actually take. Free for 3 days — no card required.
This page is legal information, not legal advice. Code text is sourced from official publications and may lag amendments — always confirm at the official source linked above. Plain-English summaries and relationship data are AI-derived and reviewed on an ongoing basis; verify with a licensed attorney before acting.