Search Results for keywords:"American Federation of Musicians

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Search Results: keywords:"American Federation of Musicians

  • Type:Notice
    Citation:90 FR 15445
    Reading Time:about 8 minutes

    The U.S. Department of Commerce has preliminarily found that Gujarat Fluorochemicals Limited (GFCL), an Indian producer and exporter of granular PTFE resin, received countervailable subsidies during 2023. These subsidies are financial contributions from authorities that benefit GFCL. Interested parties are invited to submit their comments on these preliminary findings through public filings within 21 days after the notice is published. The department plans to release more detailed calculations and assessments and will direct U.S. Customs to manage duties based on the final results.

    Simple Explanation

    The U.S. government is checking if a company from India got special help to make and sell a type of plastic, and they want people to share their thoughts on this.

  • Type:Presidential Document
    Citation:86 FR 6821
    Reading Time:about 7 minutes

    The Executive Order 13981, issued by President Donald J. Trump, focuses on protecting the United States from security risks associated with Unmanned Aircraft Systems (UAS) made by foreign adversaries. The order outlines steps to prevent the use of taxpayer money for buying UAS that present security threats, calls for assessments of current government UAS use, and encourages prioritizing domestically produced UAS. It defines "covered UAS" as those manufactured or containing components from nations like China, Russia, Iran, and North Korea and emphasizes examining how these systems are used by federal agencies. The order also directs agencies to consider replacing these UAS in future budgets.

    Simple Explanation

    The President made a rule to keep the country safe by being careful with drones that might come from places we don't fully trust, like China or Russia. He asked government teams to check if they are using these drones and to think about using ones made at home instead.

  • Type:Notice
    Citation:89 FR 100976
    Reading Time:about 10 minutes

    The U.S. Department of Commerce has found that certain aluminum foil products from Oman were sold in the U.S. at prices below their normal value during the review period from November 1, 2022, to October 31, 2023. The aluminum foil from Oman is the subject of an ongoing administrative review, specifically focusing on Oman Aluminium Rolling Company. Interested parties can submit comments on the preliminary findings, and the Commerce Department will release final results within 120 days of this preliminary publication. The outcome of this review will influence future duty assessments and deposits.

    Simple Explanation

    The U.S. government found that some shiny silver sheets from Oman were sold for too little money in the U.S., and they are deciding what to do about it. People can give their opinion now and the final decision will come soon, changing how much tax is paid for these sheets.

  • Type:Notice
    Citation:89 FR 100965
    Reading Time:about 10 minutes

    The U.S. Department of Commerce is reviewing the sale of certain aluminum foil from Brazil, finding that it was sold in the U.S. at prices below normal value between November 1, 2022, and October 31, 2023. This review is part of an antidumping duty action and involves companies like CBA Itapissuma Ltda. and Companhia Brasileira de AlumΓ­nio. Interested parties can comment on these preliminary findings, and the final results are expected within 120 days of the notice's publication. The findings will influence future duty assessments on these products.

    Simple Explanation

    The U.S. said that some aluminum foil from Brazil was sold too cheaply in the U.S. between November 2022 and October 2023, and they are thinking about adding extra charges to fix this. People who care about this can share their thoughts before a final decision is made in about four months.

  • Type:Notice
    Citation:89 FR 106515
    Reading Time:about 7 minutes

    The Food and Drug Administration (FDA) announced the release of final guidance titled "E11A Pediatric Extrapolation," prepared with the International Council for Harmonisation. This guidance aims to streamline pediatric drug development, focusing on strategies like safety extrapolation and statistical methodologies to ensure safe, effective medicines for children. It replaces a draft guidance from August 2022 and includes updates to study designs and modeling approaches. The public can comment on this guidance, which is accessible through FDA's regulations website.

    Simple Explanation

    The FDA, which makes sure medicines are safe, has shared new instructions to help make medicines for kids. They have worked with an international group to make the process faster and safer, using special math tools to predict outcomes.

  • Type:Notice
    Citation:86 FR 6979
    Reading Time:about 33 minutes

    The Department of Veterans Affairs (VA) is establishing a new system of records called the Community Care Provider Profile Management System (PPMS), as required by the Privacy Act of 1974. This system will maintain records of non-VA health care providers participating in VA community care programs. The information stored in this system includes providers' personal and professional details, such as name, contact information, and identification numbers. The VA outlines several routine uses for this information, primarily involving disclosure to appropriate agencies for purposes like verifying provider credentials or responding to legal requests, all while ensuring compliance with privacy laws like HIPAA.

    Simple Explanation

    The Department of Veterans Affairs is making a new system to keep track of doctors who help their patients, and they promise to keep the information safe and share it only when really needed.

  • Type:Notice
    Citation:86 FR 1531
    Reading Time:about a minute or two

    The Copyright Royalty Judges have received a notice from SoundExchange, Inc. to audit the royalty payments made by Rockbot, Inc.'s Business Establishment Service for the years 2017, 2018, and 2019. This audit ensures compliance with the statutory licensing terms for digital audio transmissions, as per the Copyright Act. SoundExchange is responsible for collecting and distributing these royalties to the rightful owners and performers. The notice of intent to audit was submitted on December 18, 2020, and this summary fulfills the requirement to publish in the Federal Register.

    Simple Explanation

    The people in charge of music royalties got a letter saying they will check the money Rockbot, Inc. paid musicians for playing their songs in 2017, 2018, and 2019. This is to make sure everything is fair and correct.

  • Type:Notice
    Citation:89 FR 106504
    Reading Time:about 7 minutes

    The Food and Drug Administration (FDA) has released a draft guidance document titled "M15 General Principles for Model-Informed Drug Development." This document was created under the International Council for Harmonisation (ICH) and provides recommendations on planning, evaluating, and documenting evidence in drug development using models. It aims to help harmonize regulations globally, enhancing drug development and improving manufacturing standards. Public comments on the draft can be submitted until February 28, 2025.

    Simple Explanation

    The FDA wrote a guide to help scientists use special models when making new medicines, so everyone around the world can agree on the best ways to do this. People can share their thoughts about it until February 2025, but the guide might be a little tricky to understand because it uses big words and doesn't always explain what they mean.

  • Type:Rule
    Citation:86 FR 11632
    Reading Time:about 11 minutes

    The Department of Labor has decided to delay the implementation of the Tip Regulations Under the Fair Labor Standards Act (FLSA) until April 30, 2021. This decision follows a directive for a "Regulatory Freeze Pending Review" to ensure that the rule's legal, policy, and factual issues are fully assessed. Many stakeholders during a public comment period supported the delay, expressing concerns that the rule might have complicated effects on workers, including tip credit application and compliance costs for employers. The decision also allows time to address a legal complaint arguing that certain aspects of the rule are contrary to existing laws.

    Simple Explanation

    The government decided to wait a little longer before making some new tip rules for workers and businesses to start, so they can make sure everything about the rules is okay and fair. People worry about how the rules might affect everyone, and this extra time lets them check everything again.

  • Type:Notice
    Citation:89 FR 106519
    Reading Time:about 8 minutes

    The Food and Drug Administration (FDA) is announcing the availability of a draft guidance titled "E6(R3) Good Clinical Practice: Annex 2." This document was developed with the International Council for Harmonisation (ICH) and provides guidance for conducting clinical trials with decentralized and pragmatic elements, while using real-world data. The aim is to encourage innovative trial designs and to focus on critical aspects that affect participant safety and data reliability. Comments on the draft can be submitted until February 28, 2025, before the final version is prepared.

    Simple Explanation

    The FDA has a new draft plan that helps make sure clinical trials, like tests for new medicines, are done safely and use real-world data, with a focus on keeping people safe and making sure the results are trustable. People can share their thoughts on this plan until February 2025 before it becomes final.