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Filing a DMF for Fujicalin with the U.S. FDA

Filing a drug master file (DMF) for Fujicalin can be a useful mechanism to market your Fujicalin to the U.S. Drug Industry. Typical Fujicalin producers who have filed a DMF for Fujicalin include:

  - Fuji Chemical Industrial Co Ltd

Registrar Corp can help you to properly prepare and submit your Fujicalin DMF to FDA.

As your Agent, Registrar Corp will perform the following administrative functions:

  - Format, assemble and deliver your Fujicalin DMF to FDA
  - Submit letters of authorization regarding your Fujicalin to FDA
 - Provide changes, additions and maintenance of your Fujicalin DMF
  - Respond to issues relating to ownership of your Fujicalin DMF
  - Assist with submission of responses to FDA concerning your Fujicalin DMF
  - Perform any required annual updates for your Fujicalin DMF

For more information about filing a DMF for Fujicalin, simply click below:




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U.S. FDA Regulations:

U.S. FDA DMF Regulation: 21 C.F.R. Section 314.420


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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