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Filing a DMF for Edible Inks with the U.S. FDA

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

  - Qualicaps Co Ltd

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

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

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

For more information about filing a DMF for Edible Inks, 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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