AndersonBrecon, Inc. DBA PCI Pharma Services has applied for DEA registration as an importer of controlled substances; details on specific drug classes are available in supplementary information.
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.
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.
DOJ's Justice Management Division seeks OMB approval to revise its Self Reportable Activities information collection under the Paperwork Reduction Act of 1995; public comments requested.
AndersonBrecon, Inc. DBA PCI Pharma Services has applied for DEA registration as an importer of controlled substances; supplementary information provides details on specific drug classes.
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.
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.
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.
HHS Office of Disease Prevention and Health Promotion solicits public comments on proposed Healthy People 2030 objectives and screen time measures to inform national health goals.
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