Search Results for keywords:"Federal eRulemaking Portal"

The Occupational Safety and Health Administration (OSHA) is asking for public feedback on its plan to continue collecting information required by the Personal Protective Equipment (PPE) Standard for Shipyard Employment. This proposal aims to extend the Office of Management and Budget’s (OMB) approval for these paperwork requirements. They are particularly interested in comments on the necessity and usefulness of this information, ways to reduce the burden on employers, and the accuracy of the estimated time and costs involved. Comments must be submitted by April 29, 2025, and can be sent electronically through the Federal eRulemaking Portal.

The Department of Homeland Security (DHS), through U.S. Citizenship and Immigration Services (USCIS), is inviting public comments on a proposed extension of an existing information collection regarding the Application for Provisional Unlawful Presence Waiver of Inadmissibility (Form I-601A). This notice allows an additional 30 days for comments concerning the necessity and efficiency of this information collection, which aids USCIS in determining an applicant’s eligibility for the waiver. Public feedback is requested on matters such as the collection's estimated burden and any potential improvements, and comments must be submitted by March 29, 2021, via the Federal eRulemaking Portal. The submission of Form I-601A is crucial for individuals seeking to qualify for the provisional waiver process concerning unlawful presence inadmissibility, affecting about 63,000 respondents with a total estimated annual public burden of 168,210 hours and a cost burden of $3,212,390.

Pharmaron Manufacturing Services (US), LLC has applied to the Drug Enforcement Administration (DEA) to become a bulk manufacturer of certain controlled substances. This registration is intended to allow the company to produce materials for clinical trials. Interested parties can submit comments or request a hearing on the application by May 27, 2025, via the Federal eRulemaking Portal. The application was officially filed on February 11, 2025, and no other activities related to these substances are authorized beyond clinical trial production.

The Animal and Plant Health Inspection Service of the USDA is reopening the comment period for a proposed rule regarding the US Swine Health Improvement Plan. This program aims to enhance biosecurity, traceability, and disease monitoring in swine health. The comment period will now extend until March 31, 2025, giving people more time to share their thoughts on the proposal. Individuals can submit their comments through the Federal eRulemaking Portal or by postal mail.

Organic Consultants LLC, doing business as Cascade Chemistry, has applied to the Drug Enforcement Administration (DEA) to become a bulk manufacturer of certain controlled substances. Interested parties have until April 1, 2025, to submit comments or objections regarding the application or to request a hearing. Comments can be submitted electronically through the Federal eRulemaking Portal. The company intends to produce small amounts of these substances for internal use or to sell as analytical reference standard materials, with no other activities authorized for these drug codes.

The U.S. Coast Guard is asking for public comments on its plan to continue collecting information about load lines for certain vessels, a process that makes sure ships are not overloaded. This request is part of the Paperwork Reduction Act, and the Coast Guard wants feedback on how necessary and burdensome this data collection is. Comments must be submitted by April 9, 2025, through the Federal eRulemaking Portal or by mailing them to the Coast Guard and the Office of Management and Budget (OMB). The Coast Guard emphasizes that these comments will help determine whether this information collection should be approved and if there are ways to improve its effectiveness or reduce its burden.

Pharmaron Manufacturing Services (US) LLC has applied to be registered as an importer of certain controlled substances. The Drug Enforcement Administration (DEA) announced this application and is inviting comments and requests for hearings from other registered bulk manufacturers and applicants until April 25, 2025. The company aims to use the imported substances for analytical purposes and production processes but is not authorized for commercial sale of finished dosage forms. The submission of comments should be done electronically through the Federal eRulemaking Portal.

Kinetochem LLC has filed an application to be registered as a bulk manufacturer of certain controlled substances. The company plans to manufacture these substances, including synthetic versions of Marihuana and Tetrahydrocannabinols, for use as Active Pharmaceutical Ingredients in research and clinical trials. The public or other manufacturers may submit comments or objections electronically by February 4, 2025, through the Federal eRulemaking Portal.

The Foreign Agricultural Service, part of the USDA, is planning to request an extension for a currently approved information collection concerning the Emerging Markets Program, as per the Paperwork Reduction Act of 1995. This program involves collecting information from applicants seeking grants to evaluate the viability of proposed projects and ensure compliance with statutory requirements. Public comments on this proposal must be submitted by May 5, 2025, via mail, email, or the Federal eRulemaking Portal. The estimated public reporting burden for respondents is about 6.4 hours per response, with an annual total burden of 2,100 hours.

SpecGx LLC has applied to the Drug Enforcement Administration (DEA) to become an importer of certain controlled substances. The company aims to import these substances for the purpose of manufacturing Active Pharmaceutical Ingredients, which will then be distributed to its customers. However, this registration does not automatically allow for permit applications to import these substances to be approved; approval will be granted only if the business activities comply with specific legal requirements. Public comments or requests for a hearing regarding this application are open until April 28, 2025, and can be submitted electronically through the Federal eRulemaking Portal.