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.
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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.
Farm Service Agency requests public comments on revised information collection requirements for Emergency Conservation Program and Biomass Crop Assistance Program eligibility, cost-share agreements, and payment certification.
Center for Scientific Review amended notice of meeting regarding federal grant review procedures; specific meeting date and location available upon request to the NIH.
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.
Center for Scientific Review will hold closed meetings to review and discuss NIH grant applications and related administrative matters on specified dates.
USDA APHIS is preparing a programmatic environmental impact statement for grasshopper and Mormon cricket suppression across seventeen western states, with the final document expected by August 2027.
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