Search Results for keywords:"Federal eRulemaking Portal"

The National Center for Natural Products Research has applied to the Drug Enforcement Administration (DEA) to become a registered bulk manufacturer of specific controlled substances. Specifically, they intend to manufacture these substances for product development and reference standards. The controlled substances include drug codes 7360 (Marihuana) and 7370 (Tetrahydrocannabinols), which will be isolated from Marihuana Extract (7350), but no cultivation of marihuana is authorized. Interested parties have until February 11, 2025, to submit comments or request a hearing on this application.

The Occupational Safety and Health Administration (OSHA) is seeking public comments on its proposal to renew the information collection requirements under the Temporary Labor Camp Standard. This renewal is part of efforts to ensure data collected is useful and efficiently formatted while minimizing the burden on businesses. An increase in reported cases has resulted in more workers living in contractor-provided housing, prompting OSHA to request a change in burden hours from 48 to 238. Comments can be submitted electronically via the Federal eRulemaking Portal until March 3, 2025.

Janssen Pharmaceuticals, Inc. has applied to the Drug Enforcement Administration to be registered as a bulk manufacturer of certain controlled substances. The DEA has issued a notice inviting public comments or objections to this application and requests for a hearing on the matter, which must be submitted by April 21, 2025. Comments can be made electronically through the Federal eRulemaking Portal. Janssen plans to manufacture these substances for use as intermediates in sales to customers, and no other activities are allowed under this registration.

The Defense Health Agency (DHA) has announced a proposed public information collection and is inviting comments from the public. This initiative is being implemented in compliance with the Paperwork Reduction Act of 1995. The DHA is focusing on gathering feedback about the necessity, utility, and clarity of the proposed information collection and strategies to minimize the burden on respondents. Public comments will be considered until March 11, 2025, and submissions can be made through various methods including the Federal eRulemaking Portal or by mail to the Department of Defense.

The Drug Enforcement Administration (DEA) has announced that the Research Triangle Institute has applied to become a bulk manufacturer of certain controlled substances. The institute intends to produce these substances synthetically for research purposes and to provide analytical reference standards. Interested parties can submit electronic comments or objections regarding this registration by June 17, 2025, and can request a hearing by the same date. Comments are to be submitted through the Federal eRulemaking Portal at regulations.gov.

The Internal Revenue Service (IRS) published a notice announcing a petition to add sodium chlorite to the list of taxable substances. The petition was filed by Occidental Chemical Corporation and requests public comments on this potential addition, which is not yet confirmed. Sodium chlorite is primarily used in water purification, textile bleaching, and disinfecting meat processing facilities. Comments must be submitted by March 24, 2025, using the Federal eRulemaking Portal or by mail.

Restek Corporation has applied to be registered as a bulk manufacturer of certain controlled substances. The application was submitted to the Drug Enforcement Administration on February 19, 2025, and the company plans to produce synthetic versions of substances like Marihuana and Tetrahydrocannabinols for specific purposes. Interested parties can file comments or objections, or request a hearing on this registration by June 17, 2025. All submissions must be made through the Federal eRulemaking Portal.

Scottsdale Research Institute has applied to the Drug Enforcement Administration (DEA) to be registered as a bulk manufacturer of certain controlled substances. This registration will allow them to manufacture these substances for internal research and analytical development purposes only. Comments or objections regarding this application can be submitted electronically until April 21, 2025, via the Federal eRulemaking Portal. A hearing request can also be made by the same date.

The Environmental Protection Agency (EPA) has received a pesticide petition seeking to establish or modify regulations for pesticide residues on various food commodities. The EPA is inviting public comments on the petition by February 12, 2025, through the Federal eRulemaking Portal. This action mainly affects those in crop production, food manufacturing, and pesticide manufacturing sectors. The EPA has not yet assessed the sufficiency of the data provided, and more data may be required before making a final decision.

The Rural Business-Cooperative Service (RBCS) of the USDA plans to revise an existing information collection for the Rural Development Cooperative Agreements (RDCA) Program. They are inviting public comments on this proposal in accordance with the Paperwork Reduction Act of 1995. The proposed changes aim to improve the effectiveness and coordination of programs supporting rural areas. Comments can be submitted via the Federal eRulemaking Portal until February 18, 2025.