The Federal Communications Commission's Enforcement Bureau affirms that civil forfeiture penalties will not be adjusted for inflation in 2026 under the Federal Civil Penalties Inflation Adjustment Act Improvements Act of 2015.
National Institutes of Health seeks 30-day public comments on proposed information collection forms for the Genetic Testing Registry before submitting to Office of Management and Budget for approval.
National Institutes of Health Director's Office holds a public meeting to discuss agency policies and operations affecting biomedical research funding and grant administration.
Federal Communications Commission modernizes the Disaster Information Reporting System to streamline reporting for communications service providers during disasters while expanding coverage to public safety networks.
FDA classifies skin patches for hyperhidrosis treatment as Class II medical devices, requiring special controls to ensure safety and effectiveness while expediting patient access to the technology.
The Centers for Medicare & Medicaid Services re-establishes a matching program with the Peace Corps to verify eligibility for minimum essential coverage under the Affordable Care Act through Peace Corps health benefit plans.
Center for Scientific Review closed meeting on May 22, 2025 to discuss peer review procedures and personnel matters related to grant applications and program administration.
FDA classifies monitors for opioid-induced impairment of oxygenation as class II medical devices, subject to special controls to ensure safety and effectiveness.
FDA classifies medial knee implanted shock absorbers as Class II devices subject to special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
FDA determines the regulatory review period for VYALEV human drug product patent extension purposes and publishes this notice as required by law.
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