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.
Department of Labor seeks OMB approval for an information collection regarding Employee Benefit Security Administration rules on prohibited transaction exemptions for employer customer notes; public comment period is open.
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.
FEMA seeks public comment on paperwork collection extensions for Homeland Security Exercise and Evaluation Program documentation including After Action Reports, Integrated Preparedness Plans, and Support Request Forms used to validate national prepa…
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