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.
Statement of Organization for HHS Office for Civil Rights defines departmental structure, functions, and delegated authorities for civil rights enforcement and compliance.
FDA classifies monitors for opioid-induced impairment of oxygenation as class II medical devices, subject to special controls to ensure safety and effectiveness.
World Trade Center Health Program denies eight petitions to add ischemic heart disease conditions to the List of WTC-Related Health Conditions due to insufficient evidence.
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 agencies must submit information collection requests to OMB for review and public comment, with submissions subject to the Paperwork Reduction Act approval process.
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 medial knee implanted shock absorbers as Class II devices subject to special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
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