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.
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.
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.
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.
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.
Medicare's final rule strengthens oversight of accrediting organizations by addressing conflicts of interest, establishing consistent standards, and updating validation systems for deemed providers and suppliers across multiple care settings.
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.
Proposed rule codifies Medicare Drug Price Negotiation Program under the Inflation Reduction Act of 2022 and establishes new policies for drug benefit programs and fixed combination drugs.
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