The Department of Health and Human Services requests technical input on pharmacy benefit manager compensation and data practices to implement legislative restrictions and reporting requirements effective January 1, 2028.
CMS is requesting public comment on proposed information collection activities under the Paperwork Reduction Act; interested parties may submit feedback on burden estimates and collection methods.
The Federal Communications Commission invites public comment on information collection requirements under the Paperwork Reduction Act, with specific attention to reducing burdens on small businesses with fewer than 25 employees.
FDA seeks 60 days of public comment on information collection requirements for extralabel drug use in animals under the Paperwork Reduction Act.
FDA submission to OMB for Paperwork Reduction Act review of information collection requirements for dietary supplement manufacturing, packaging, labeling, and holding operations.
FDA requests OMB clearance for information collection activities related to Current Good Manufacturing Practice regulations for Type A medicated articles and medicated feeds under the Paperwork Reduction Act of 1995.
The FDA renews its Science Board advisory committee for an additional two years, with the new charter expiring June 26, 2028.
FDA withdraws approval of SpecGx LLC's abbreviated new drug application for Methylphenidate Hydrochloride Extended-Release tablets in 27mg, 36mg, and 54mg strengths per the applicant's request.
FDA issues Emergency Use Authorizations for two animal drugs to prevent and treat New World screwworm infestations in livestock, poultry, and exotic animals following HHS's August 18, 2025 public health emergency declaration.
FCC seeks public comment on information collection burdens and specifically invites small businesses with fewer than 25 employees to suggest paperwork reduction measures under the Small Business Paperwork Relief Act of 2002.
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