Search Results for keywords:"Federal eRulemaking Portal"

The Office of Workers' Compensation Programs (OWCP) announced a bulletin titled "DCMWC Self-Insurance Process Guidelines" that outlines updates to their process for evaluating self-insurance applications under the Black Lung Benefits Act. This act requires coal mine operators to either purchase insurance for benefits or get authorization from the Department of Labor to self-insure. The bulletin detailing these updates is open for public comment until February 8, 2021, and interested parties can submit comments through the Federal eRulemaking Portal. OWCP's goal is to ensure that coal operators are financially responsible for benefits, minimizing reliance on the Black Lung Disability Trust Fund.

Scottsdale Research Institute has applied to the Drug Enforcement Administration (DEA) to become a bulk manufacturer of certain controlled substances. This registration is intended to support the production of these substances for clinical trials and research purposes. The public can submit comments or objections electronically through the Federal eRulemaking Portal by April 21, 2025. The DEA requires comments to be submitted online and will provide a tracking number to confirm submission.

The U.S. Coast Guard is asking for public comments on extending the approval of information collection related to Drawbridge Operation Regulations. The Coast Guard collects information from bridge owners to change the operating schedules of drawbridges over U.S. navigable waters, as per 33 U.S.C. 499. They estimate the process involves an annual burden of 1,672 hours. Comments on this proposal can be submitted online until February 11, 2021, via the Federal eRulemaking Portal or other specified channels.

The Office of the Under Secretary of Defense for Research and Engineering (OUSD(R&E)) has announced a proposed information collection and is seeking public comments, as required by the Paperwork Reduction Act of 1995. The objective is to gather feedback on the necessity, utility, and burden of the data collection process. Interested individuals can submit their comments until March 11, 2025, via the Federal eRulemaking Portal or by mail. The information collected will be used to monitor federal awards, evaluate progress, manage scientific programs, and prepare reports. The expected annual burden of this collection is 24,000 hours, involving 2,000 respondents providing responses twice a year.

The U.S. Coast Guard is seeking public feedback on extending the approval for an information collection about displaying fire control plans on commercial vessels. This information helps firefighters and damage control efforts during emergencies. The Coast Guard invites the public to comment on the necessity, utility, accuracy, and potential burden of this data collection. Comments must be submitted by April 9, 2025, through the Federal eRulemaking Portal or the Office of Management and Budget's (OMB) website.

Patheon API Services Inc. has applied to the Drug Enforcement Administration (DEA) to become a registered bulk manufacturer of certain controlled substances. This registration is intended to support the clinical trials of their customers. Interested parties are invited to submit comments or objections electronically through the Federal eRulemaking Portal by June 17, 2025. They may also request a hearing on the application by the same date.

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.

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.

Patheon Pharmaceuticals Inc. has applied to the Drug Enforcement Administration to become a registered bulk manufacturer of certain controlled substances. The company plans to use these substances as Active Pharmaceutical Ingredients in FDA-approved medications. Anybody interested can submit comments or objections electronically by May 12, 2025, through the Federal eRulemaking Portal. Requests for a hearing regarding this application are also due by the same date.

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.