Code of Federal Regulations (CFR) : Pharmaguideline
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  • Jul 16, 2021

    Code of Federal Regulations (CFR)

    Code of Federal Regulations (CFR) is a part of Federal Register that has codification of the rules and regulations for different departments.
    The Code of Federal Regulations (CFR) is the codification of the general and permanent rules and regulations (sometimes called administrative law) distributed in the Federal Register by the executive departments, leader offices, and agencies of the Federal Government of the United States. The Office of the Federal Register, also known as the agency of the National Archives and Records Administration (NARA) publishes the CFR.

    The CFR is split into 50 titles that address extensive areas subject to federal regulations.
    Every year each volume is updated and issued every quarter are as follow:

    Title 1-16 1st January
    Title 17-27 1st April
    Title 29-41 1st July
    Title 42-50 1st October
    • The change of color of each set of volumes takes place every year.
    • Each title is separated into chapters, which as a rule bear the name of the issuing agency.
    • Each chapter is sub-divided into parts that enclose specified regulatory areas.
    • Large parts may be subdivided into subparts. All parts are organized in sections.
    • CFR titles are separated by Chapter, Subchapter, and Part.
    Before foregoing, let us know each part is a Table of Contents for the individual guidelines contained inside that part.

    List of Regulation Titles
    Title 1:General Provisions
    Title 2:Grants and Agreements
    Title 3: The President
    Title 4: Accounts
    Title 5: Administrative Personnel
    Title 6: Homeland Security
    Title 7: Agriculture
    Title 8: Aliens and Nationality
    Title 9: Animals and Animal Products
    Title 10: Energy
    Title 11: Federal Elections
    Title 12: Banks and Banking
    Title 13: Business Credit and Assistance
    Title 14: Aeronautics and space
    Title 15: Commerce and Foreign Trade
    Title 16: Commercial Practices
    Title 17: Commodity and Securities Exchanges
    Title 18: Conservation of Power and Water Resources
    Title 19: Customs Duties
    Title 20: Employees Benefits
    Title 21: Food and Drugs (administered by the US Food and Drug Enforcement Administration)
    Title 22: Foreign Relations
    Title 23: Highways
    Title 24: Housing and Urban Development
    Title 25: Indians
    Title 26: Internal Revenue
    Title 27: Alcohol, Tobacco Products and Firearms
    Title 28: Judicial Administration
    Title 29: Labor
    Title 30: Mineral Resources
    Title 31: Money and Finance: Treasury
    Title 32: National Defense
    Title 33: Navigation and Navigable Waters
    Title 34: Education
    Title 35: Reserved (formerly Panama Canal)
    Title 36: Parks, Forests, and Public Property
    Title 37: Patents and Trademarks and Copyrights
    Title 38: Pensions, Bonuses and Veterans Relief
    Title 39: Postal Service
    Title 40: Protection of environment
    Title 41: Public contracts and Property Management
    Title 42: Public health
    Title 43: Public lands interior
    Title 44: Emergency management and assistance
    Title 45: Public welfare
    Title 46: Shipping
    Title 47: Telecommunication
    Title 48: Federal acquisition regulations system
    Title 49: Transportation
    Title 50: Wildlife and Fisheries

    Title 21- Food and drugs inside the United States is governed by this portion (Title 21) of the CFR for the Food and Drug Administration (FDA). This index is composed of PARTS 200-299. 210 and 211, deal with cGMP.
    210- Current Good Manufacturing Practice in manufacturing, processing, packing, or holding of drugs
    211- Current Good Manufacturing Practice for finished pharmaceuticals.

    Part 210 is composed of the following sections:
    210.1- This section contains the Status of current good manufacturing practice regulation
    210.2- This section holds on the Applicability of current good manufacturing practice regulations
    210.3- This section deals with Definitions

    Part 211 consists of sub-parts A to K. They are as follow:
    Subpart A-General provisions
    Subpart B- Organization and personnel
    Subpart C- Buildings and Facilities
    Subpart D-Equipment
    Subpart E- Control of components and drug product containers and closures
    Subpart F- Production and process controls
    Subpart G- Packaging and labeling control
    Subpart H- Holding and distribution
    Subpart I- Laboratory controls
    Subpart J- Records and reports
    Subpart K- Returned and salvaged drug products

    Part 211 contains subparts, which contains sections like:
    Subpart A-General Provisions
    211.1 - Scope
    211.3- Definitions
    Subpart B- Organization and Personnel
    211.22-Responsibilities of a quality control unit
    211.25- personnel qualifications
    211.28- personnel responsibilities
    211.34- consultants

    Why is CFR of Prior Importance?
    All federal departments and agencies produce CFRs so that the public and government officials are aware of the changes in regulations and also they get updates on literally every subject that the federal government has jurisdiction to manage. These constantly updated federal regulations can unfold fantastic opportunities for the general public. CFRs are updated on a routine basis based upon new federal legislation, changes in economic or social objectives.

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