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.
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.
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.
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.
EPA releases draft risk evaluation of flame retardant TBBPA under TSCA and requests public comment on whether the chemical presents unreasonable health or environmental risks under current use conditions.
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.
The EPA will transfer pesticide product data and claimed confidential business information to the Department of Justice and litigation parties under FIFRA and FFDCA disclosure rules.
NMFS issues two consecutive 1-year incidental harassment authorizations to the U.S. Navy for marine mammal takes during the S50S/LNG and S499 Bulkheads Replacement Project at Naval Station Newport, Rhode Island.
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