Food & Drug Administration
The Food & Drug Administration regulates the safety of drugs, medical devices and diagnostics used across the care continuum.
What FDA does
The main responsibilities of the Food & Drug Administration.
Working with FDA
Track device and medication safety notices relevant to your services
Keep equipment, calibration and recall records organised
Link safety alerts to the teams and settings they affect
Sectors, programs & frameworks
The care sectors, federal programs and regulatory frameworks most connected to FDA. Applicability varies by provider type, program and jurisdiction.
Federal programs
Not tied to a specific funding program.
Regulatory frameworks
- CLIA — Federal standards for clinical laboratory testing.
Alongside federal agencies, US care is also shaped by state licensure, survey agencies and Medicaid programmes across all 50 states. Explore the 50-state directory for state-level intelligence.
One platform, from federal government to the front line
CareFocusIQ connects agencies, programs, states and sectors into a single intelligent platform for US care.
CareFocusIQ provides technology and intelligence to support care operations and compliance. It is not a medical device and does not provide legal advice. Regulatory requirements vary by provider type, program and jurisdiction, and remain the responsibility of each provider.