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Hazardous Waste Worker Training OMB Comment Request 42 CFR Part 65

NIH/NIEHS published a corrected notice reopening the 30-day public comment period for an information collection request regarding hazardous waste worker training under 42 CFR Part 65. The original notice was published on March 18, 2026. This correction notice extends the comment period for stakeholders to provide feedback on the proposed training requirements for workers handling hazardous waste.

Routine Notice Environmental Protection
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ACIP Charter Renewal Notice

The CDC renewed the Advisory Committee on Immunization Practices (ACIP) charter through April 2028. This routine administrative notice confirms the committee's continued operation under its federal advisory committee mandate. No new policy requirements or compliance obligations are established.

Routine Notice Public Health
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Reducing Bureaucracy and Burden for Children, Youth, and Family Programs

The Administration for Children and Families (ACF) within HHS has published a proposed rule to reduce bureaucratic burden and administrative requirements for programs serving children, youth, and families. The rule aims to streamline regulations affecting child welfare, foster care, youth development, and family support programs. Public comments are being accepted through May 6, 2026.

Priority review Consultation Social Services
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E2B(R3) Data Standards for Postmarketing Safety Reports

FDA issued a notice proposing updated E2B(R3) data standards for electronic submission of postmarketing individual case safety reports to the FDA Adverse Event Monitoring System. The notice introduces new regional data elements and establishes an implementation schedule. Comments are due by October 1, 2026 (180 days from publication).

Priority review Notice Pharmaceuticals
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STRATTERA Not Withdrawn for Safety or Effectiveness

The FDA determined that STRATTERA (atomoxetine hydrochloride) capsules at all dosage strengths (5mg through 100mg) were not withdrawn from sale for reasons of safety or effectiveness. This determination allows generic drug manufacturers to reference this finding in abbreviated new drug applications (ANDAs) without providing separate safety and effectiveness data.

Routine Notice Pharmaceuticals
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Icebreaker Collaboration Effort (ICE) Pact Request for Information

The Maritime Administration (MARAD) published a Request for Information (RFI) seeking public input on the Icebreaker Collaboration Effort (ICE) Pact, a potential initiative for collaboration on icebreaker ship construction. The agency is soliciting feedback from industry stakeholders, shipbuilders, and other interested parties. The comment period closes on June 5, 2026.

Routine Consultation Transportation
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FTZ 21 Production Activity - Turbocam Turbine Components

The Foreign-Trade Zones Board published notice 91 FR 17245 requesting public comment on Turbocam Inc.'s proposed production activity at FTZ 21 in Ladson, South Carolina. The company seeks authority to manufacture turbine system components under the FTZ program. The Board invites public comments on the proposed activity.

Routine Notice International Trade
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Bank Control Notice Correction Regarding Share Acquisitions

The Federal Reserve published a correction to its Change in Bank Control Notices regarding acquisitions of shares of banks and bank holding companies. The document (91 FR 17278) corrects errors in a previously published notice. This is a routine correction with no new regulatory requirements or substantive changes to existing policy.

Routine Notice Banking
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Bank Holding Company Formations, Acquisitions, and Mergers

The Federal Reserve System published a notice listing recent formations of bank holding companies and acquisitions/mergers approved or processed under the Bank Holding Company Act. This routine notice provides public awareness of ownership changes in the banking sector. No specific transactions, deadlines, or penalties are detailed in this notice.

Routine Notice Banking
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PIC/S GMP Guide Revised Chapters 3, 5, 8 and Annex 17

PIC/S has revised Chapters 3, 5, 8 and Annex 17 of the GMP Guide (PE 009-14), aligning them with EU GMP principles and Quality Risk Management. Key changes include new cross-contamination prevention requirements in Chapters 3 and 5, updated supplier qualification requirements, and expanded quality defect evaluation expectations in Chapter 8. The revision entered into force on 1 July 2018.

Priority review Rule Pharmaceuticals

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