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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 263 regulations

US21 CFR21 CFR Part 1402Secondary 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 526Secondary legislationIn force

Intramammary Dosage Form New Animal Drugs

4 days ago

US21 CFR21 CFR Part 529Secondary legislationIn force

Certain Other Dosage Form New Animal Drugs

4 days ago

US21 CFR21 CFR Part 868Secondary legislationIn force

Anesthesiology Devices

4 days ago

US21 CFR21 CFR Part 514Secondary legislationIn force

New Animal Drug Applications

4 days ago

US21 CFR21 CFR Part 511Secondary legislationIn force

New Animal Drugs for Investigational Use

4 days ago

US21 CFR21 CFR Part 888Secondary legislationIn force

Orthopedic Devices

4 days ago

US21 CFR21 CFR Part 1321Secondary legislationIn force

DEA Mailing Addresses

4 days ago

US21 CFR21 CFR Part 515Secondary legislationIn force

Medicated Feed Mill License

4 days ago

US21 CFR21 CFR Part 1107Secondary legislationIn force

Exemption Requests and Substantial Equivalence Reports

4 days ago

US21 CFR21 CFR Part 874Secondary legislationIn force

Ear, Nose, and Throat Devices

4 days ago

US21 CFR21 CFR Part 866Secondary legislationIn force

Immunology and Microbiology Devices

4 days ago

US21 CFR21 CFR Part 864Secondary legislationIn force

Hematology and Pathology Devices

4 days ago

US21 CFR21 CFR Part 814Secondary legislationIn force

Premarket Approval of Medical Devices

4 days ago

US21 CFR21 CFR Part 820Secondary legislationIn force

Quality Management System Regulation

4 days ago

US21 CFR21 CFR Part 1105Secondary legislationIn force

General

4 days ago

US21 CFR21 CFR Part 860Secondary legislationIn force

Medical Device Classification Procedures

4 days ago

US21 CFR21 CFR Part 822Secondary legislationIn force

Postmarket Surveillance

4 days ago

US21 CFR21 CFR Part 861Secondary legislationIn force

Procedures for Performance Standards Development

4 days ago

US21 CFR21 CFR Part 821Secondary legislationIn force

Medical Device Tracking Requirements

4 days ago

US21 CFR21 CFR Part 810Secondary legislationIn force

Medical Device Recall Authority

4 days ago

US21 CFR21 CFR Part 808Secondary 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

Mandatory Declassification Review

Interstate Conveyance Sanitation

Biological Products: General

Unique Device Identification

Minimum Required Warning Statements

In Vitro Diagnostic Products for Human Use

Repurchase, Repairs, or Replacement of Electronic Products

Neurological Devices

Obstetrical and Gynecological Devices

Ophthalmic Devices

Regulations Under the Federal Caustic Poison Act

Ophthalmic and Topical Dosage Form New Animal Drugs

General and Plastic Surgery Devices

Additional Standards for Miscellaneous Products

Cosmetic Product Warning Statements

Gastroenterology-Urology Devices

Cardiovascular Devices

Dental Devices

Clinical Chemistry and Clinical Toxicology Devices

Extralabel Drug Use in Animals

Tolerances for Residues of New Animal Drugs in Food

Intentional Genomic Alterations in Animals

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

Intramammary Dosage Form New Animal Drugs

Certain Other Dosage Form New Animal Drugs

Anesthesiology Devices

New Animal Drug Applications

New Animal Drugs for Investigational Use

Orthopedic Devices

DEA Mailing Addresses

Medicated Feed Mill License

Exemption Requests and Substantial Equivalence Reports

Ear, Nose, and Throat Devices

Immunology and Microbiology Devices

Hematology and Pathology Devices

Premarket Approval of Medical Devices

Quality Management System Regulation

General

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