01 · United States
FDA
Federal regulator
Reviews evidence for safety, effectiveness, manufacturing quality, and indication-specific labeling.
Open the individual record →The Imperial Bureau
Regulators and reviewers who decide which claimed miracles may legally become medicines
02 · European Union
EMA
European regulator
Coordinates scientific evaluation and supervision of medicines across the European Union.
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03 · Every jurisdiction
The Inspection Desk
Quality and compliance
Asks the unglamorous questions about identity, sterility, manufacturing, labeling, and adverse events.
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