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FDA Modernization Act 3.0 : report (to accompany H.R. 2821).
Connect to full text Available online
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- Book
- Government document
- Author/Creator:
- United States. Congress. House. Committee on Energy and Commerce, author.
- Series:
- United States. Congress. House. Report ; 119-706.
- Report / 119th Congress, 2d session, House of Representatives ; 119-706
- Language:
- English
- Subjects (All):
- United States. Food and Drug Administration--Rules and practice.
- United States.
- Public health laws--United States.
- Public health laws.
- Drugs--Law and legislation--United States.
- Drugs.
- Cosmetics--Law and legislation--United States.
- Cosmetics.
- Food law and legislation--United States.
- Food law and legislation.
- Genre:
- Legislative materials.
- Physical Description:
- 1 online resource (65 pages)
- Other Title:
- Food and Drug Administration Modernization Act 3
- Place of Publication:
- [Washington, D.C.] : [U.S. Government Publishing Office], [2026]
- Notes:
- In scope of the U.S. Government Publishing Office Cataloging and Indexing Program (C&I) and Federal Depository Library Program (FDLP).
- "June 18, 2026."
- This is a publication issued by the United States federal government or produced with federal funds.
- Referred bill: H.R. 2821.
- Includes bibliographical references.
- Description based on online resource, PDF version; title from title page (GovInfo, viewed July 9, 2026).
- Other Format:
- Print version: United States. Congress. House. Committee on Energy and Commerce. FDA Modernization Act 3.0
- OCLC:
- 1602857035
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