50 Electronic Codes of Federal Regulation (e-CFR) in pharma

As per FDA there are 50 title of Electronic Codes Of Federal Regulation (E-CFR) In Pharmaceutical.

In this article we will see the all 50 title of electronic code of federal regulation.

Electronic Codes Of Federal Regulation (E-CFR) In Pharma

Out of 50 codes, 21 Code is represented to the Food and Drugs (21 CFR). In FDA, Code is term as a title according to that 21 Title is Food and Drugs.

Codes of Federal Regulation (CFR) are:

Title 1: General Provisions

Title 2: Grants and Agreements

Title 3: President

Title 4: Accounts

Title 5: Administrative Personnel

Title 6: Domestic 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: Aeronautical 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

Title 22: Foreign Relations

Title 23: Highways

Title 24: Housing and Urban Developement

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 36: Park, Forest and Public Property

Title 37: Patents, Trademarks and Copyrights

Title 38: Pentions, Bonuces, and Veteran’s Relief

Title 39: Postal Service

Title 40: Protection and Environment

Title 41: Public Contracts and Property Management

Title 42: Public Health

Title 43: Public Lands: Interior

Title 44: Emergency Management and Assiatance

Title 45: Public Welfare

Title 46: Shipping

Title 47: Telecommunication

Title 48: Federal Acquisition and Regulations System

Title 49: Transportation

Title 50: Wildlife and Fisheries

These are total 50 Title as per Federal regulation.

Also Read:

Difference Between 21 CFR Part 11 and EU Annex 11

ICH 14 Guidelines in pharmaceutical

Title 21 is a Food and Drugs well-known as 21 CFR.

CFR Title 21 has three main chapters;

Chapter I: Food and Drug Administration, Department of Health and Human Services (Subchapters A to L )

Chapter II: Drug Enforcement Administration, Department of Justice (Parts 1300-1322-1399)

Chapter III: Office of National Drug Control Policy (Part 1400-1403-1499)

Chapter I: Food and Drug Administartion, Department of Health and Human Services (Subchapters A to L )

In Chapter I there are Subchapters from A to L as mention below;

Subchapters From A to L

Subchapter A: General Parts (1-99). 21 CFR Part 11 comes under this subchapter.

Subchapter B: Food for Human Consumption (Parts 100-191-199)

Subchapter C: Drugs : General ( Parts 200-299)

Subchapter D: Drugs for Human Use ( Parts 300-377-499)

Subchapter E: Animal drugs, Feed, and Related Products. ( Parts 500-590-599)

Subchapter F: Biologics ( Parts 600-680)

Subchapter G: Cosmetics ( Parts 700-741-799)

Subchapter H: Medical Devices (Parts 800-898)

Subchapter I: Mammography Quality Standard Act ( Parts 900)

Subchapter J: Radiological Health ( Parts 1000-1050)

Subchapter K: Tobacco Products ( Parts 1100-1150)

Subchapter L: Regulations Under Certain Other Acts Administered By The Food and Drug Administration (Parts 1210-1272-1299)

Also Read:

Contamination, Cross-contamination and mix-ups in pharma

For Interview Preparation: Refer Interview Q&A

YT channel: Refer Pharmabeej