The full form of CFR in pharmacy is the Code of Federal Regulations.
The Code of Federal Regulations (CFR) is a compilation of the general and permanent rules and regulations (administrative law) published in the Federal Register by the executive departments and agencies of the U.S. Federal Government. It is essentially a codification of federal laws, organized by subject matter. In the context of pharmacy, the CFR contains regulations related to the manufacturing, distribution, dispensing, and labeling of drugs, as well as other aspects of pharmaceutical practice and healthcare. It is a critical resource for pharmacists, pharmaceutical companies, and regulatory agencies to ensure compliance with federal laws.
For instance, a pharmacist might consult the CFR to understand regulations concerning compounding sterile preparations or to determine the requirements for prescription labeling. Pharmaceutical manufacturers rely on the CFR to ensure that their manufacturing processes adhere to Good Manufacturing Practices (GMP) as outlined by the FDA.
In summary, the Code of Federal Regulations is a key resource for understanding and adhering to the laws and regulations governing the pharmaceutical industry and pharmacy practice in the United States.
