Global regulations corpus

Browse 11,703 regulations from 34 regulators

1,774 updated in the last 30 days. Public corpus — no signup required to read.

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Showing 151–200 of 241 regulations

US21 CFR21 CFR Part 530Secondary legislationIn force

Extralabel Drug Use in Animals

4 days ago

US21 CFR21 CFR Part 607Secondary legislationIn force

Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices

4 days ago

US21 CFR21 CFR Part 556Secondary legislationIn force

Exemptions from Federal Preemption of State and Local Medical Device Requirements

4 days ago

US21 CFR21 CFR Part 812Secondary legislationIn force

Investigational Device Exemptions

4 days ago

US21 CFR21 CFR Part 710Secondary legislationIn force

Voluntary Registration of Cosmetic Product Establishments

4 days ago

US21 CFR21 CFR Part 720Secondary legislationIn force

Voluntary Filing of Cosmetic Product Ingredient Composition Statements

4 days ago

US21 CFR21 CFR Part 800Secondary legislationIn force

General

4 days ago

US21 CFR21 CFR Part 806Secondary legislationIn force

Medical Devices; Reports of Corrections and Removals

4 days ago

US21 CFR21 CFR Part 807Secondary legislationIn force

Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices

4 days ago

US21 CFR21 CFR Part 801Secondary legislationIn force

Labeling

4 days ago

US21 CFR21 CFR Part 803Secondary legislationIn force

Medical Device Reporting

4 days ago

US21 CFR21 CFR Part 640Secondary legislationIn force

Additional Standards for Human Blood and Blood Products

4 days ago

US21 CFR21 CFR Part 630Secondary legislationIn force

Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use

4 days ago

US21 CFR21 CFR Part 660Secondary legislationIn force

Additional Standards for Diagnostic Substances for Laboratory Tests

4 days ago

US21 CFR21 CFR Part 700Secondary legislationIn force

General

4 days ago

US21 CFR21 CFR Part 601Secondary legislationIn force

Licensing

4 days ago

US21 CFR21 CFR Part 589Secondary legislationIn force

Substances Prohibited from Use in Animal Food or Feed

4 days ago

US21 CFR21 CFR Part 610Secondary legislationIn force

General Biological Products Standards

4 days ago

US21 CFR21 CFR Part 898Secondary legislationIn force

Performance Standard for Electrode Lead Wires and Patient Cables

4 days ago

US21 CFR21 CFR Part 606Secondary legislationIn force

Current Good Manufacturing Practice for Blood and Blood Components

4 days ago

US21 CFR21 CFR Part 573Secondary legislationIn force

Food Additives Permitted in Feed and Drinking Water of Animals

4 days ago

US21 CFR21 CFR Part 584Secondary legislationIn force

Food Substances Affirmed as Generally Recognized as Safe in Feed and Drinking Water of Animals

4 days ago

US21 CFR21 CFR Part 579Secondary legislationIn force

Irradiation in the Production, Processing, and Handling of Animal Feed and Pet Food

4 days ago

US21 CFR21 CFR Part 570Secondary legislationIn force

Food Additives

4 days ago

US21 CFR21 CFR Part 571Secondary legislationIn force

Food Additive Petitions

4 days ago

US21 CFR21 CFR Part 515Secondary legislationIn force

Medicated Feed Mill License

4 days ago

US21 CFR21 CFR Part 522Secondary legislationIn force

Implantation or Injectable Dosage Form New Animal Drugs

4 days ago

US21 CFR21 CFR Part 701Secondary legislationIn force

Cosmetic Labeling

4 days ago

US21 CFR21 CFR Part 582Secondary legislationIn force

Substances Generally Recognized as Safe

4 days ago

Extralabel Drug Use in Animals

Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices

Tolerances for Residues of New Animal Drugs in Food

New Animal Drugs for Use in Animal Feeds

Intramammary Dosage Form New Animal Drugs

Clinical Chemistry and Clinical Toxicology Devices

Certain Other Dosage Form New Animal Drugs

New Animal Drug Applications

Orthopedic Devices

New Animal Drugs for Investigational Use

Exemption Requests and Substantial Equivalence Reports

Anesthesiology Devices

Ear, Nose, and Throat Devices

Immunology and Microbiology Devices

Hematology and Pathology Devices

Premarket Approval of Medical Devices

General

Quality Management System Regulation

Medical Device Classification Procedures

Postmarket Surveillance

Procedures for Performance Standards Development

Medical Device Tracking Requirements

Medical Device Recall Authority

Exemptions from Federal Preemption of State and Local Medical Device Requirements

Investigational Device Exemptions

Voluntary Registration of Cosmetic Product Establishments

Voluntary Filing of Cosmetic Product Ingredient Composition Statements

General

Medical Devices; Reports of Corrections and Removals

Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices

Labeling

Medical Device Reporting

Additional Standards for Human Blood and Blood Products

Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use

Additional Standards for Diagnostic Substances for Laboratory Tests

General

Licensing

Substances Prohibited from Use in Animal Food or Feed

General Biological Products Standards

Performance Standard for Electrode Lead Wires and Patient Cables

Current Good Manufacturing Practice for Blood and Blood Components

Food Additives Permitted in Feed and Drinking Water of Animals

Food Substances Affirmed as Generally Recognized as Safe in Feed and Drinking Water of Animals

Irradiation in the Production, Processing, and Handling of Animal Feed and Pet Food

Food Additives

Food Additive Petitions

Medicated Feed Mill License

Implantation or Injectable Dosage Form New Animal Drugs

Cosmetic Labeling

Substances Generally Recognized as Safe