Top 25 When Was The Code Of Federal Regulations Created Update

The Code of Federal Regulations (CFR) is a comprehensive compilation of federal regulations in the United States. It is meticulously maintained and published by the Office of the Federal Register, which operates under the jurisdiction of the National Archives and Records Administration. The CFR undergoes updates, rather than complete publication, approximately once each calendar year. These updates follow a staggered schedule in line with the annual update cycle. As of September 9, 2022, the CFR was current and up-to-date. This means that the CFR is continuously evolving to incorporate new regulations and changes, ensuring it remains a vital resource for understanding the legal framework governing various aspects of American life.

The Code of Federal Regulations (CFR) in the pharmaceutical industry is a comprehensive compilation of enduring regulations initially published in the Federal Register by various executive departments and federal agencies within the U.S. government. It serves as a vital reference document outlining legal requirements and guidelines governing various aspects of pharmaceutical manufacturing, safety, and distribution. Specifically, Title 21 within the CFR is exclusively designated for regulations established and enforced by the Food and Drug Administration (FDA). This section of the CFR is particularly significant for the pharmaceutical sector as it details the specific rules and standards pharmaceutical companies must adhere to in order to ensure the safety, quality, and efficacy of drugs and medical products. Please note that the original passage lacked a publication date, so it’s essential to verify the most recent CFR updates to stay compliant with the latest regulatory changes.