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The Environmental Protection Agency (EPA) is seeking public comments on a proposed extension for collecting information related to pesticide use, as required by specific sections of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). This process involves collecting information from various entities like states and federal agencies about emergency exemptions for unregistered pesticide use and special local needs for additional pesticide uses. The current approval for this information collection expires on February 28, 2021, and the EPA is offering an additional 30-day period for public feedback. The estimated annual burden for respondents, which include state and federal government agencies and agricultural chemical manufacturers, is 25,753 hours, costing a total of $1,829,103.

The U.S. Environmental Protection Agency (EPA) has finalized amendments to the Standards of Performance for Volatile Organic Liquid Storage Vessels, initially established for storage vessels built after July 23, 1984. These amendments now allow operators of storage vessels with external or internal floating roofs to optionally comply with the National Emission Standards for Storage Vessels (Tanks)—Control Level 2, which can reduce volatile organic compound (VOC) emissions by preventing the need to empty and degas tanks for inspections. The rule is expected to save costs and decrease environmental impact without sacrificing inspection rigor. The final rule went into effect on January 19, 2021.

The document from the Centers for Medicare & Medicaid Services (CMS) corrects errors in a previous rule regarding payment systems and reporting programs for hospitals and surgical centers. These corrections involve fixing technical and typographical mistakes in tables, payment rates, and website links. Changes also include adjusting codes and figures related to payment systems and Medicare policies. The document clarifies that these adjustments ensure accurate payments and reflect the policies without altering underlying methodologies.

The Centers for Disease Control and Prevention (CDC) is seeking public comments on a proposal concerning the collection of information related to COVID-19 tests for airline passengers entering the United States. This proposal requires passengers to present either a negative COVID-19 test taken within three days before their flight or documentation of recovery from the virus. There are some exemptions, such as for certain federal personnel and urgent humanitarian cases. The CDC aims to prevent COVID-19 transmission while acknowledging the potential costs and efforts involved in implementing these requirements.

The Environmental Protection Agency (EPA) has finalized a rule under the Federal Clean Water Act to amend the California Toxics Rule by establishing a revised selenium water quality criterion for certain freshwater bodies in California. This new criterion aims to protect aquatic life and wildlife that depend on these aquatic ecosystems from high selenium levels, which can be toxic. The EPA incorporated public feedback and scientific evidence into the rule, and it includes measures to account for site-specific conditions. The rule will take effect on January 16, 2025, unless California develops its own compliant standards.

The Department of Labor (DOL) is seeking public comments on its proposed Information Collection Request (ICR) submitted to the Office of Management and Budget (OMB) for review. This request is part of the Paperwork Reduction Act of 1995 and relates to the collection of data to ensure nondiscrimination in programs funded by DOL. The document invites feedback on several aspects of the information collection process and is open for comments until February 16, 2021. The goal is to ensure fair practices while streamlining and improving the information collection methods.

The U.S. Department of Homeland Security (DHS) has delayed the implementation of a new rule regarding the H-1B visa selection process until December 31, 2021. This rule intended to change how H-1B visa applications are selected, focusing on using wage levels for prioritization. The delay allows U.S. Citizenship and Immigration Services (USCIS) additional time to update and test their systems and train their staff to ensure a smooth transition, avoiding confusion and operational disruptions. During this delay, H-1B registrations for the fiscal year 2022 will follow the existing random selection process.

The Environmental Protection Agency (EPA) has requested approval from the Office of Management and Budget for a new information collection related to its Environmental Justice Collaborative Problem Solving (EJCPS) and Government to Government (EJG2G) programs. These programs aim to support projects that address environmental and public health challenges by collaborating with community-based organizations and local governments, especially in underserved communities. The EPA plans to collect progress and final reports from grant recipients to evaluate project effectiveness and equity. Public comments on this information collection are open until February 18, 2025.

The Department of Commerce is seeking comments from the public on the National Survey of Children's Health (NSCH), as they prepare to submit information collection requests to the Office of Management and Budget (OMB). This survey, conducted by the U.S. Census Bureau, gathers important data to estimate the health and wellbeing of children nationwide, focusing on those with special health care needs. There are two modes of data collection: an online survey and a mail-in paper survey. Public comments on this information collection are welcomed to help reduce paperwork burdens and improve the process before the final submission to OMB.

The Food and Drug Administration (FDA) has issued a final rule establishing new guidelines for nonprescription drugs that require an "Additional Condition for Nonprescription Use" (ACNU). This rule allows drugs that can't be safely used with labeling alone to be sold without a prescription if the manufacturer implements an approved ACNU to ensure proper use. It aims to expand consumer access to certain drugs that would otherwise need a prescription and outlines specific requirements for drug application, labeling, and reporting failures of the ACNU process. The rule will take effect on January 27, 2025, and is intended to improve public health by making more medications safely available as nonprescription options.