Center for Scientific Review will hold closed meetings to review research grant applications and provide advice on scientific matters to the National Institutes of Health.
Department of Commerce seeks 60 days of public comment on information collection requirements for Coastal Zone Management Program Administration before submitting to OMB under the Paperwork Reduction Act.
NMFS implements shallow-water grouper catch limits and recreational closed seasons for Gulf of America fisheries to reduce scamp and yellowmouth grouper harvest pending Amendment 58A development.
The FDA issues a final 5-year debarment order against Andrew Jonathan Morgan, prohibiting him from importing or offering for import any drug into the United States based on a federal felony conviction related to drug importation.
FDA classifies radiological machine learning-based quantitative imaging software with predetermined change control plans as Class II medical devices, subject to special controls to ensure safety and effectiveness.
FDA classifies ingestible gastrointestinal blood detection capsules as class II devices, establishing special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
USDA amends Title VI Civil Rights Act regulations to eliminate disparate-impact liability and align with Department of Justice standards under Executive Order 14281, reducing compliance costs for regulated entities.
Center for Scientific Review amended notice of meeting for the National Institutes of Health scientific review group; meeting details and date available in Federal Register notice.
Center for Scientific Review will hold closed meetings to review grant applications and personnel matters; specific dates and locations available upon request to the designated agency contact.
FDA corrects withdrawal of approval for 11 abbreviated new drug applications; Masuu Global Solutions LLC's propranolol and lidocaine ANDAs remain approved as of March 23, 2026.
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