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Filing a DMF for Galactomannan C (Davanat) with the U.S. FDA

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

  - Sigma Aldrich Manufacturing Llc

Registrar Corp can help you to properly prepare and submit your Galactomannan C (Davanat) DMF to FDA.

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

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

For more information about filing a DMF for Galactomannan C (Davanat), 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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