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HomeDrugsU.S. FDA Active Pharmaceutical Ingredients (API)API Examples › U.S. FDA Regulations: Urokinase

U.S. FDA Requirements: Urokinase

In the United States, Urokinase is regulated by the U.S. Food and Drug Administration (FDA). FDA has specific requirements regarding the registration and listing of Urokinase.

Registrar Corp assists Urokinase companies with:

  • FDA Registration Urokinase
  • FDA Listing Urokinase
  • FDA Label Requirements and Exceptions Urokinase
  • FDA Import Information Urokinase
  • FDA Detentions Urokinase (Urokinase Entry Refusal)
  • General U.S. Food and Drug Administration Guidelines for:
       - Manufacturers Urokinase (Urokinase Suppliers)
       - Processors Urokinase
       - Repackers Urokinase
       - Relabelers Urokinase
       - Exporters Urokinase
       - Importers Urokinase
For more information about Urokinase, simply click below:

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U.S. FDA Regulations:

U.S. FDA Regulation: 21 C.F.R. Part 207

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
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