Major Update to Title 21 of the Code of Federal Regulations: A Look at “Food and Drugs” as of August 15, 2025
We are pleased to inform you of a significant publication from govinfo.gov, the official repository for U.S. government publications. As of August 15, 2025, at 16:07, the Code of Federal Regulations (CFR) has been updated to include Title 21 – Food and Drugs. This comprehensive update reflects the latest regulatory landscape governing the safety, efficacy, and labeling of food and drug products in the United States.
Title 21 of the CFR is a cornerstone of public health regulation, overseen primarily by the Food and Drug Administration (FDA). It meticulously outlines the rules and standards that manufacturers, distributors, and marketers must adhere to throughout the lifecycle of food, drugs, cosmetics, and medical devices. This latest publication represents a crucial snapshot of these regulations, incorporating any amendments, revisions, or new provisions that have come into effect.
What This Update Means:
For stakeholders across the food and drug industries, this August 15, 2025, publication is an essential resource. It signifies the most current and authoritative version of Title 21, providing critical guidance on a wide array of topics, including but not limited to:
- Food Safety Standards: Regulations pertaining to Good Manufacturing Practices (GMPs), hazard analysis and critical control points (HACCP), food labeling requirements, and standards for specific food products.
- Drug Approval and Regulation: The complex processes for new drug applications (NDAs), investigational new drug applications (INDs), drug manufacturing standards, labeling requirements for prescription and over-the-counter (OTC) drugs, and post-market surveillance.
- Cosmetics: Regulations concerning the safety, labeling, and manufacturing of cosmetic products.
- Medical Devices: Standards for the design, manufacturing, labeling, and marketing of medical devices, including classification and pre-market review processes.
- Dietary Supplements: Guidelines and regulations for the manufacturing and labeling of dietary supplements.
The availability of this updated Title 21 on govinfo.gov underscores the government’s commitment to transparency and accessibility of crucial regulatory information. Professionals in these sectors are encouraged to review the updated content to ensure full compliance with the latest federal requirements.
How to Access the Updated Information:
The official publication can be accessed directly through the govinfo.gov website. Users can navigate to the specific entry for Title 21, Food and Drugs, as published on August 15, 2025. govinfo.gov offers robust search capabilities, allowing users to find specific sections, regulations, or keywords within the vast body of the CFR.
This update serves as a valuable reminder of the dynamic nature of regulatory frameworks designed to protect public health and ensure the integrity of the products we consume and use. We encourage all relevant parties to familiarize themselves with this important publication.
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