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The Federal Railroad Administration (FRA), part of the Department of Transportation (DOT), has set up an emergency relief docket (ERD) for 2021, identified as docket number FRA-2021-0001. This ERD streamlines the process for handling requests for waivers from safety rules during emergencies. If an emergency event occurs, the FRA Administrator can activate special procedures to provide relief to the railroad industry. Individuals can search for comments related to any docket online, and the FRA has privacy policies in place for these exchanges.

The Food and Drug Administration (FDA) is establishing a public docket to gather comments about using a Type V Drug Master File (DMF) for submitting Model Master Files (MMFs) in support of Abbreviated New Drug Applications (ANDAs). MMFs contain detailed information about computer-simulated models used in drug development. The FDA is seeking feedback from the public and interested parties to improve the sharing and acceptance of these models. Comments must be submitted electronically or in writing by April 17, 2025.

The Food and Drug Administration (FDA) is announcing a public advisory committee meeting involving the Arthritis Advisory Committee and the Drug Safety and Risk Management Advisory Committee. This meeting, which will be held online due to COVID-19, is set for March 24-25, 2021. During the meeting, the committees will discuss a drug application by Pfizer for a treatment targeting moderate to severe osteoarthritis. The FDA has established a public docket to gather comments on regulatory issues, which will remain open until March 23, 2021.

The Federal Railroad Administration (FRA), part of the Department of Transportation, has established an emergency relief docket (ERD) for 2025, identified as docket number FRA-2025-0015. This announcement is part of FRA's process for handling emergency waivers of safety rules during crises. If an emergency occurs, the FRA Administrator can activate special procedures to provide relief to the railroad industry, which will be announced and updated on the FRA's website. Public comments on petitions for emergency waivers can be submitted through the regulations.gov portal, where they will be accessible to the public.