FCC Debars Ben Klein from E-Rate and USF Programs

The FCC Enforcement Bureau has issued a debarment notice against Ben Klein, prohibiting him from participating in the E-Rate and other Universal Service Fund (USF) programs. This action follows related enforcement actions against individuals involved in E-Rate fraud.

FCC Debars Simon Goldbrener from E-Rate Programs

The FCC Enforcement Bureau has debarred Simon Goldbrener from participating in E-Rate and other Universal Service Fund programs. This action follows related enforcement actions against individuals involved in E-Rate fraud.

FCC Debars Peretz Klein from E-Rate and USF Programs

The FCC Enforcement Bureau has debarred Peretz Klein from participating in activities related to the E-Rate and Universal Service Fund (USF) programs. This action follows related enforcement actions against other individuals involved in E-Rate fraud.

ISDA Responds to FCA Consultation on Derivatives Transparency

ISDA has responded to the UK Financial Conduct Authority's (FCA) consultation CP26/8 regarding transparency requirements for financial instruments. The response supports a proposed change to MAR 11 to resolve a discrepancy between OTC derivatives in scope for public transparency and the permissible CFI codes.

Tran et al v. Pham et al - Defend Trade Secrets Act Case

The U.S. District Court for the Northern District of California has a new filing in the civil case Tran et al v. Pham et al, concerning a Defend Trade Secrets Act claim. Recent filings include motions to file documents under seal related to a preliminary injunction.

SEC Application of Federal Securities Laws to Crypto Assets

The SEC and CFTC have issued a final rule clarifying the application of federal securities laws to certain crypto assets and related transactions. This rule aims to provide greater certainty for market participants regarding regulatory obligations.

Burnett v. AstraZeneca Pharmaceuticals LP - Employment Retaliation

The Fourth Circuit affirmed a district court's grant of summary judgment in favor of AstraZeneca Pharmaceuticals LP in an employment case brought by Tiffany Burnett. The court found that Ms. Burnett's claims for retaliation and violations of the Equal Pay Act lacked sufficient evidence to proceed.

Palazzo v. Bayview Loan Servicing LLC - Debt Collection in Bankruptcy

The Fourth Circuit affirmed a district court's decision in favor of Bayview Loan Servicing LLC and M&T Bank. The court found that communications sent to a debtor during Chapter 13 bankruptcy proceedings did not constitute prohibited debt collection activities and that the calculations within the documents were not inaccurate under federal or state consumer protection laws.

Center for Vein Restoration Settles False Claims Allegations for $4 Million

Connecticut, along with other states and the federal government, has reached a $4 million settlement with CVR Management, LLC, resolving allegations that its network of clinics billed government health programs for medically unnecessary vein treatments. CVR will pay $4 million, with Connecticut receiving $114,280.07 for its Medicaid program.

CT AG Joins 8 States to Block Nexstar-TEGNA Merger

Connecticut Attorney General William Tong, joined by eight other state attorneys general, has filed an emergency motion to stop the merger between Nexstar Media Group and TEGNA Inc. The merger, which received regulatory approval from the FCC and DOJ, is expected to create the largest broadcast station group in the US, potentially leading to job cuts and increased consumer costs.

FDA Variance Renewal from Lapis Lasers & Lighting FX

The FDA has posted a variance renewal request from Lapis Lasers & Lighting FX, LLC. The document is available for review and download via the Regs.gov portal. No specific details on the variance itself are provided in the metadata.

FDA Complaint Document

The FDA has posted a complaint document related to its regulatory activities. No content is available for viewing or download, but an attachment labeled 'Complaint' is provided by the CTP author.

FDA Variance Approval Letter to Mykyta Sukhenko

The FDA's Center for Devices and Radiological Health (CDRH) has issued a variance approval letter to Mykyta Sukhenko. The document is restricted due to personally identifiable information, but a redacted version is available.

FDA Variance Application from Mykyta Sukhenko

The FDA has posted a variance application submitted by Mykyta Sukhenko. The application is restricted due to personally identifiable information, but a redacted version is available for review. This notice serves to inform the public of the application's existence.

FDA Variance Approval Letter for Vault Entertainment Inc.

The Food and Drug Administration (FDA) has issued a variance approval letter to Vault Entertainment Inc. This document grants a specific variance related to regulatory requirements. The FDA's Center for Devices and Radiological Health (CDRH) authored the letter.

FDA Acknowledgment Letter to Kyle Cummings

The FDA has posted an acknowledgment letter sent to Kyle Cummings regarding a submission. The letter is from the FDA's Division of Management and Budget (DMB) and was authored by CDRH. A redacted version is available for download.

FDA Variance Approval Letter to Laser Wizardry

The FDA has issued a variance approval letter to Laser Wizardry regarding a medical device. This document is part of the regulatory process for medical device manufacturers seeking specific approvals or variances from standard requirements.

FDA Variance Approval Letter

The FDA's Center for Devices and Radiological Health (CDRH) has issued a variance approval letter. The document is restricted due to Personally Identifiable Information and a redacted version is available for download.

FDA Acknowledges Letter from 3 Foot World

The FDA has acknowledged receipt of a letter from 3 Foot World regarding a matter associated with docket FDA-2026-V-1589. The agency has provided a link to the acknowledgment letter, which was authored by CDRH.

FDA Complaint Document

The FDA has posted a complaint document related to its regulatory activities. The document is available for review on the Regs.gov platform. No specific details about the nature of the complaint or the parties involved are provided in the metadata.

FDA Variance Application from Life to the Full, LLC

The FDA has posted a variance application from Life to the Full, LLC. The application details are available via a link on the Regs.gov portal. No documents are currently available for direct viewing or download.

FDA Variance Application from Matthew Lewis

The FDA has posted a variance application submitted by Matthew Lewis, with redacted information available for download. This application is related to medical device regulations and was submitted through CDRH.

FDA Variance Approval Letter for Alexander Kulik

The FDA has issued a variance approval letter to Alexander Kulik, as posted on March 20, 2026. The letter, issued by the Center for Devices and Radiological Health (CDRH), pertains to a specific variance request.

FDA Acknowledgment Letter to Mykyta Sukhenko

The Food and Drug Administration (FDA) has posted an acknowledgment letter sent to Mykyta Sukhenko regarding a submission. The letter, authored by the Center for Devices and Radiological Health (CDRH), indicates a formal receipt of information or documentation.

FDA Variance Approval Letter to 3 Foot World

The FDA's Center for Devices and Radiological Health (CDRH) has issued a variance approval letter to 3 Foot World. The document indicates a specific approval for a variance related to a medical device. No further details on the nature of the variance or its implications are provided in the metadata.

FDA Variance Approval Letter to Feral Artisans

The FDA has issued a variance approval letter to Feral Artisans regarding a medical device. The document is available for download and further information can be accessed via the provided link.

FDA Complaint Document

The FDA has closed a complaint document for public comment. The document is related to the Center for Tobacco Products (CTP) and is available for review on regulations.gov. No specific compliance deadlines or actions are detailed in this notice.

FDA Variance Application from Vault Entertainment Inc.

The FDA has received a variance application from Vault Entertainment Inc. The document is a filing related to a variance request, with no downloadable content available directly in the provided feed entry. Further details are available via the provided URL.

FDA Variance Application from Alexander Kulik

The FDA has posted a variance application submitted by Alexander Kulik. The application is from the CDRH (Center for Devices and Radiological Health) and has been redacted for personally identifiable information. The document is available for review on Regs.gov.

FDA Acknowledgment Letter to Life to the Full, LLC

The Food and Drug Administration (FDA) has issued an acknowledgment letter to Life to the Full, LLC. This letter confirms receipt of a submission from the company. The FDA's Center for Devices and Radiological Health (CDRH) is listed as an author.

FDA Variance Application from Illuminate Production Services

The FDA has posted a variance application from Illuminate Production Services. The document is available for review on Regs.gov, with the application submitted by CDRH.

FDA Variance Application from Kyle Cummings

The FDA has posted a variance application submitted by Kyle Cummings. The application is from the CDRH (Center for Devices and Radiological Health) and is available for review, with a redacted version provided for download. No specific details of the variance are available in the provided text.

FDA Variance Approval Letter to Kyle Cummings

The FDA has issued a variance approval letter to Kyle Cummings, as posted on March 20, 2026. The document is restricted due to personally identifiable information and was authored by CDRH.

FDA Response Letter for Docket FDA-2026-P-0529

The FDA has posted a response letter related to docket FDA-2026-P-0529. The document was authored by the Center for Veterinary Medicine (CVM) and is available for download. No other details or specific actions are indicated.

Marquis Software Solutions Data Breach Notice to Consumers

The Vermont Attorney General's Office has published a data breach notice from Marquis Software Solutions to consumers. The notice, dated March 16, 2026, informs consumers about a data security incident affecting their personal information. Specific details regarding the nature of the breach or affected data were not provided in the summary document.

Electric Bicycles Trade Remedies Investigation

The European Commission has initiated a new export producer treatment review investigation concerning electric bicycles. This investigation, case NEPT20-08, was initiated on February 17, 2026, and will examine potential trade remedies related to electric bicycles.

Haskell County Insurance Producer Fined, License Revoked

The Oklahoma Insurance Department has fined and revoked the license of Leslie Clark, an insurance producer from Haskell County, for misappropriating $7,269.38 in consumer premium payments. The action follows an investigation by the OID's Anti-Fraud Unit and a failure to appear at a show-cause hearing.

West Virginia WIOA State Plan Mid-Cycle Update Public Comment

The State of West Virginia is seeking public comment on its mid-cycle update to the 2024-2027 WIOA State Plan. The comment period is open from March 20, 2026, to April 20, 2026.

OFAC Adds Persons to SDN List

The Office of Foreign Assets Control (OFAC) has added new persons to the Specially Designated Nationals (SDN) List. These individuals and entities are blocked, and U.S. persons are prohibited from engaging in transactions with them due to their support for HAMAS.

NYSE Arca Rule Filing SR-NYSEARCA-2026-26 - Colocation Services

The NYSE Arca has filed a rule change (SR-NYSEARCA-2026-26) concerning colocation services, specifically for NY11-5. The filing, published in the Federal Register, makes new cabinet and power options available on a non-discriminatory basis. The rule change became effective immediately upon filing, with the SEC waiving the standard 30-day operative delay.

SBA Reporting and Recordkeeping Requirements Under OMB Review

The Small Business Administration (SBA) has published a notice regarding reporting and recordkeeping requirements currently under review by the Office of Management and Budget (OMB). This notice opens a comment period for the public to provide input on these requirements.

Presidential Declaration Amendment for Mississippi Disaster Assistance

The Small Business Administration (SBA) issued a notice amending a presidential declaration for major disaster assistance in Mississippi. This amendment specifically pertains to public assistance for the state and the Mississippi Band of Choctaw Indians.

Rate Adjustments for Indian Irrigation Projects

The Bureau of Indian Affairs has announced rate adjustments for Indian irrigation projects. This notice provides information on these adjustments and opens a public comment period for interested parties.

Correction of Public Land Order No. 7963 Withdrawal in New Mexico

The Department of the Interior's Bureau of Land Management issued a correction to Public Land Order No. 7963, which pertains to a withdrawal in Doña Ana, Luna, and Hidalgo Counties, New Mexico. This notice clarifies specific details related to the original withdrawal.

FDA National Priority Voucher Pilot Program Public Hearing Request

The FDA is announcing a public hearing regarding its National Priority Voucher Pilot Program. The hearing will be held on June 12, 2026, and is intended to gather public input on the program. Registration details and requests for participation are available on the FDA website.

FDA Proposed Collection for Animal Drug User Fees

The Food and Drug Administration (FDA) has published a proposed collection of information regarding animal drug and animal generic drug user fees. This notice initiates a public comment period for the proposed reporting requirements associated with these user fees.

FDA Seeks Comment on Advisory Committee Information Collection

The Food and Drug Administration (FDA) is requesting public comment on its proposed collection of information related to advisory committee activities. This notice initiates a comment period for stakeholders to provide feedback on the agency's information collection requests concerning these committees.

NFA Clarifies Affiliate Lending Rules for Commodity Pool Operators

The National Futures Association (NFA) has adopted amendments to Rule 2-45, effective March 16, 2026, to clarify affiliate lending arrangements for commodity pool operators (CPOs). These changes expand circumstances under which CPOs may lend pool assets to affiliates, introducing new compliance and recordkeeping obligations, particularly for large, regulated investment managers.

IRS Internal Revenue Bulletin 2026-13

The IRS published Internal Revenue Bulletin 2026-13, including proposed regulations on electronic furnishing of payee statements for digital asset sales by brokers and guidance on a new pilot program for child accounts. The bulletin also includes a notice requesting comments on modifying electronic furnishing requirements for brokers and other persons.

Digital Euro Benefits and Pilot Plans

The European Central Bank (ECB) outlined the benefits and pilot plans for a digital euro, emphasizing its role in enhancing European payment autonomy and resilience. A 12-month pilot program is scheduled to begin in the second half of 2027, involving selected payment service providers, merchants, and Eurosystem staff.