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Federal Regulations

How Congress's laws become real-world rules. Browse regulatory dockets from Regulations.gov — tracking rulemaking activity, public comment periods, and the agencies turning legislation into policy.

Dockets
6,540
Regulations.gov

Showing 30 of 6,540 dockets

Rulemaking
MSHA

MSHA_FRDOC_0001

Notice Proposed Information Collection Request; Submitted for Public Comment and Recommendations; Ventilation Plans, Tests, and Examinations in Underground Coal Mines

0 docsNo comments
Rulemaking
TREAS

TREAS_FRDOC_0001

Financial Crimes Enforcement Network; Anti-Money Laundering Programs; Special Due Diligence Programs for Certain Foreign Accounts RULES

309 docsNo comments
Nonrulemaking
FDA

FDA-2001-N-0047

Progress on Implementing for the Common Technical Document

2 docsNo comments
Nonrulemaking
FDA

FDA-2001-D-0061

Submitting Marketing Applications according to ICH/CTD Format

2 docsNo comments
Nonrulemaking
FDA

FDA-2026-H-3162

DAB Civil Money Penalty; Midtown Smoke Shop Inc. d/b/a Midtowne Smoke Shop

1 docNo comments
Nonrulemaking
FDA

FDA-2026-H-1577

DAB Civil Money Penalty; Pines Road Quick Stop LLC d/b/a Get-N-Geaux / Valero; CLOSED 04/03/2026

1 docNo comments
Nonrulemaking
FDA

FDA-2001-D-0164

Guidance ICH Q1D Bracketing & Matrixing Designs for Stability

4 docsNo comments
Nonrulemaking
FDA

FDA-2026-H-2296

DAB Civil Money Penalty; Old Trail Enterprises, Inc. d/b/a Ken’s Quick Stop; CLOSED 04/03/2026

1 docNo comments
Nonrulemaking
DOD
Open for Comments

DOD-2026-OS-0034

The GlobalNET Collection; OMB Control Number 0704-0558

2 docs1 comment
Comments due Apr 28, 2026
Nonrulemaking
FDA

FDA-2001-P-0241

ANDA Suitability for Hydrocortisone Acetate Lotion, 2.5%

7 docsNo comments
Nonrulemaking
FDA

FDA-2001-P-0294

Immediately ban the Sale of Human Cadaveric Dura Mater

3 docsNo comments
Nonrulemaking
FDA

FDA-2001-Q-0320

Health Claim Notification for Foods Containing Choline Based

6 docsNo comments
Nonrulemaking
FDA

FDA-2001-P-0215

Determine Whether Sotradecol Has Been Withdrawn from Sale

2 docsNo comments
Nonrulemaking
FDA

FDA-2001-P-0153

Listing the Color Additive Yellow #5 for use in Food and Drug

2 docsNo comments
Nonrulemaking
FDA

FDA-2001-P-0158

Regulate Reprocessed Single Use Medical Devices as Reusable

1 docNo comments
Nonrulemaking
FDA

FDA-2001-N-0074

Withdrawal of 51 NDAs & 25 ANDAs

3 docsNo comments
Nonrulemaking
FDA

FDA-2001-P-0190

Revoke Invalid FDA Regulations

2 docsNo comments
Nonrulemaking
FDA

FDA-2001-P-0154

Non-lyophilized Cytoxan

5 docsNo comments
Nonrulemaking
FDA

FDA-2001-M-0022

Corometrics Model 120 F-Series Maternal/Fetal Oxygen Saturization Monitoring

1 docNo comments
Nonrulemaking
FDA

FDA-2001-P-0369

Not Rely on Non-Public Filings to Approve an Innovator NDA

2 docsNo comments
Nonrulemaking
FDA

FDA-2001-N-0203

Institutional Review Boards

3 docs52 comments
Rulemaking
EPA
Open for Comments

EPA-R05-OAR-2025-0171

Sheboygan, Wisconsin 2015 Ozone Moderate Attainment Plan

3 docsNo comments
Comments due May 5, 2026
Rulemaking
EPA
Open for Comments

EPA-R05-OAR-2025-0170

Milwaukee, Wisconsin 2015 Ozone Moderate Attainment Plan

3 docsNo comments
Comments due May 5, 2026
Rulemaking
EPA
Open for Comments

EPA-R05-OAR-2025-0169

Kenosha, Wisconsin 2015 Ozone Moderate Attainment Plan

3 docsNo comments
Comments due May 5, 2026
Rulemaking
NOAA

NOAA-NMFS-2025-0638

Taking Marine Mammals Incidental to Geophysical Surveys in the Gulf of America

6 docs36 comments
Nonrulemaking
FDA
Open for Comments

FDA-2026-P-3632

Requests that the FDA to determine that PRALIDOXIME CHLORIDE (AUTOINJECTOR) 600 mg/2 mL intramuscular solution, (NDA 018986) from Meridian Medical Technologies Inc. was not discontinued or withdrawn due to safety or efficacy reasons.

5 docsNo comments
Nonrulemaking
EPA

EPA-HQ-OW-1998-2344

Municipal Water Pollution Prevention Program Evaluation (Self-Audit)

2 docsNo comments
Rulemaking
EPA

EPA-R06-RCRA-2022-0756

Arkansas : 40 CFR Part 272 Incorporation by Reference State Hazardous Waste Management Program

1 docNo comments
Nonrulemaking
FDA
Open for Comments

FDA-2025-P-4513

Requests that the FDA amend and/or remove specific labeling and directions, explicitly; if possible, use weight to dose; from all Infant's OTC single-ingredient acetaminophen liquid drug formulations for 2-3 year of age, 24-35 lb.

9 docsNo comments
Nonrulemaking
FDA
Open for Comments

FDA-2026-P-3630

Requests that the FDA issue a declaration permitting the submission of an Abbreviated New Drug Application (ANDA) for Tamsulosin Hydrochloride Capsules, USP 0.8 mg

4 docsNo comments
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