HRSA solicits public comment on a proposed Information Collection Request for performance measures related to the Transforming Pediatrics for Early Childhood Program under the Paperwork Reduction Act of 1995.
FDA amends animal drug regulations to reflect application actions for new animal drugs during October through December 2025 and improve regulatory accuracy and readability.
This correction addresses a typographical error in the April 14, 2026 Federal Register notice regarding Medicare hospital inpatient and long-term care payment systems and quality program requirements for fiscal year 2027.
Center for Scientific Review will hold closed meetings to review and discuss National Institutes of Health grant applications and proposals.
FDA determines CHEWTADZY (tadalafil) chewable tablets were not withdrawn for safety or effectiveness reasons, enabling generic ANDA approvals for 5mg, 10mg, and 20mg formulations.
FDA approves MRESVIA respiratory syncytial virus vaccine under a rare pediatric disease priority review voucher program on June 12, 2025.
FDA approves MNEXSPIKE (COVID-19 Vaccine, mRNA) as a rare pediatric disease product eligible for priority review voucher redemption as of May 30, 2025.
CMS is accepting public comments on proposed information collection activities subject to Paperwork Reduction Act requirements; submit feedback on burden estimates and collection necessity by the specified deadline.
FDA publishes draft guidance (VICH GL8(R1)) for stability testing of medicated premixes intended for animal feed incorporation, developed through international harmonization standards.
FDA requests 60-day public comment period on information collection requirements for its prescription drug importation regulation under the Paperwork Reduction Act.
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